J. Clegg

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Structure of the zeta chain of human embryonic hemoglobin.

J. Clegg, J. Gagnon, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Plasmodium vivax: a cause of malnutrition in young children.

K. Maitland, T. Peto, J. Clegg, 1997, QJM : monthly journal of the Association of Physicians.

Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin.

F. Ismail-Beigi, J. Clegg, D. Weatherall, 1977, Journal of medical genetics.

Detection of Alpha Thalassaemia in Negro Infants

S. Higgs, J. Clegg, D. Weatherall, 1980, British journal of haematology.

Inherited haemoglobin disorders: an increasing global health problem.

D J Weatherall, J. Clegg, D. Weatherall, 2001, Bulletin of the World Health Organization.

Causes of preterm delivery and intrauterine growth retardation in a malaria endemic region of Papua New Guinea

J. Clegg, N. Alexander, S. Allen, 1998, Archives of disease in childhood. Fetal and neonatal edition.

A novel alpha-globin gene arrangement in man.

J. Clegg, D. Weatherall, D. Higgs, 1980, Nature.

β0 THALASSÆMIA—TIME FOR A REAPPRAISAL ?

J. Clegg, D. Weatherall, J. Clegg, 1974 .

Gene Duplication and Haemoglobin Polymorphism

J. Clegg, 1971 .

Direct measurement of the male recombination fraction in the human beta-globin hot spot.

J. Schneider, T. Peto, J. Clegg, 2002, Human molecular genetics.

Hemoglobin A2-Roosevelt: α2δ220ValåGlu

J. Clegg, H. Weiss, R. F. Rieder, 1976 .

α+‐Thalassaemia and pregnancy in a malaria endemic region of Papua New Guinea

J. Clegg, D. Weatherall, S. Allen, 2006, British journal of haematology.

The distribution of nascent globin chains on human reticulocyte polysomes.

J. Clegg, D. Weatherall, C. Eunson, 1971, Biochimica et biophysica acta.

Haemoglobin synthesis in beta-thalassaemia.

J. Clegg, D. Weatherall, S. Na-nakorn, 1968, Nature.

Major rearrangement in the human β-globin gene cluster

R. W. Jones, J. Clegg, D. Weatherall, 1981, Nature.

The Haemoglobin Constitution of Infants with the Haemoglobin Bart's Hydrops Foetalis Syndrome

J. Clegg, D. Weatherall, W. H. Boon, 1970, British journal of haematology.

Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

Gene deletions in alpha thalassemia prove that the 5' zeta locus is functional.

J. Clegg, D. Weatherall, D. Higgs, 1980, Proceedings of the National Academy of Sciences of the United States of America.

Haemoglobin Bart's hydrops syndrome in Greece.

J. Clegg, D. Weatherall, D. Higgs, 1980, British medical journal.

THE MOLECULAR BASIS FOR THE HAEMOGLOBIN BART'S HYDROPS FETALIS SYNDROME IN CYPRUS

J. Clegg, D. Weatherall, D. Higgs, 1981, British journal of haematology.

Alpha zero-thalassemia due to recombination between the alpha 1-globin gene and an AluI repeat.

J. Clegg, D. Weatherall, D. Higgs, 1985, Blood.

δβ-Thalassemia is due to a gene deletion

J. Clegg, D. Weatherall, W. Lanyon, 1976, Cell.

Multiple arrangements of the human embryonic zeta globin genes.

S. Goodbourn, J. Clegg, D. Weatherall, 1982, Nucleic acids research.

Globin genes in Micronesia: origins and affinities of Pacific Island peoples.

A. Hill, J. Clegg, D. Weatherall, 1990, American journal of human genetics.

Chromosomes with one, two, three, and four fetal globin genes: molecular and hematologic analysis.

A. Hill, J. Clegg, D. Weatherall, 1986, Blood.

Human haemoglobin genetics.

J. Clegg, D. Weatherall, W. Wood, 1979, Ciba Foundation symposium.

HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) AND δβ THALASSAEMIA

J. Clegg, D. Weatherall, W. Wood, 1979 .

World distribution of factor V Leiden

J. Clegg, D. Rees, M. Cox, 1995, The Lancet.

Absence of malaria-specific mortality in children in an area of hyperendemic malaria.

K. Maitland, T. Peto, J. Clegg, 1997, Transactions of the Royal Society of Tropical Medicine and Hygiene.

Molecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation.

L. Excoffier, A. Langaney, R. Harding, 2002, American journal of human genetics.

Management and Prognosis

J. Clegg, D. Weatherall, 2008 .

The Hemoglobin E Syndromes

J. Clegg, D. Weatherall, E. Vichinsky, 1998, Annals of the New York Academy of Sciences.

The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes

J. Clegg, D. Weatherall, D. Higgs, 1981, British journal of haematology.

Benign sickle-cell anaemia.

J. Clegg, D. Weatherall, M. J. Brown, 1972, British journal of haematology.

A New Sickling Disorder Resulting from Interaction of the Genes for Haemoglobin S and α‐Thalassaemia

J. Clegg, D. Weatherall, J. Blankson, 1969, British journal of haematology.

Heterocellular Hereditary Persistence of Fetal Haemoglobin (Heterocellular HPFH) and its Interaction with β Thalassaemia

J. Edwards, J. Clegg, D. Weatherall, 1977, British journal of haematology.

Highly variable regions of DNA flank the human alpha globin genes.

S. Goodbourn, J. Clegg, D. Weatherall, 1981, Nucleic acids research.

A gene tree for beta-globin sequences from Melanesia.

R. Griffiths, S. Fullerton, R. Harding, 1997, Journal of molecular evolution.

Recombination Breakpoints in the Human β-Globin Gene Cluster

J. Kidd, J. Clegg, S. Thein, 1998 .

The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1974, Nature.

Delta-beta-thalassemia is due to a gene deletion.

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

Genetic factors as determinants of infectious disease transmission in human communities.

A. Hill, J. Flint, J. Bell, 1988, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

A Genetically Determined Disorder with Features both of Thalassaemia and Congenital Dyserythropoietic Anaemia

J. Clegg, D. Weatherall, H. Knox-macaulay, 1973, British journal of haematology.

Alpha thalassaemia in British people.

A. Hill, J. Clegg, D. Weatherall, 1985, British medical journal.

Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific).

T. Vulliamy, J. Clegg, D. Weatherall, 1995, American journal of human genetics.

Distribution and Population Genetics of the Thalassaemias

J. Clegg, D. Weatherall, 2008 .

Analysis of the human a-globin gene cluster reveals a highly informative genetic locus ( haplotype / genetic linkage / recombinatlon / polymorphism )

A. Hill, J. Flint, J. Clegg, 2022 .

The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications.

J. Clegg, D. Weatherall, I. Verma, 2003, Blood cells, molecules & diseases.

Can the product of the \[thetas] gene be a real globin?

J. Clegg, 1987, Nature.

Presence of gene for β globin in homozygous β0 thalassaemia

R. Williamson, J. Clegg, D. Weatherall, 1976, Nature.

Molecular characterisation of a hypervariable region downstream of the human alpha‐globin gene cluster.

J. Clegg, A. Jarman, D. Weatherall, 1986, The EMBO journal.

Global distribution of the CCR5 gene 32-basepair deletion

J. Clegg, N. Chapman, J. Martinson, 1997, Nature Genetics.

Genetic control of F cells in human adults.

J. Clegg, D. Weatherall, M. Zago, 1979, Blood.

Polymorphism and Divergence in the (cid:98) -Globin Replication Origin Initiation Region

S. Fullerton, J. Bond, R. Harding, 1999 .

Hemoglobin H disease and mental retardation: a new syndrome or a remarkable coincidence?

D. Hunt, J. Clegg, D. Weatherall, 1981, The New England journal of medicine.

VNTR-Haplotype Associations Table I Properties of the 5 ' HVR and 3 ' HVR Loci

J. Clegg, J. Martinson, '. A. J. Boyce, 2007 .

C-Terminal Half of Immunoglobulin λ Chains

C. Milstein, J. Clegg, J. Jarvis, 1967, Nature.

Foetal erythropoiesis in human leukaemia

J. Clegg, D. Weatherall, W. Wood, 1975, Nature.

Genetic variability in response to infection: malaria and after

J. Clegg, D. Weatherall, JB Clegg, 2002, Genes and Immunity.

Haemoglobin Radcliffe (alpha2beta299(Gi)Ala): a high oxygen-affinity variant causing familial polycythaemia.

M. Perutz, C. Ho, J. Clegg, 1977, British journal of haematology.

The polyadenylation site mutation in the alpha-globin gene cluster.

J. Clegg, D. Weatherall, D. Higgs, 1988, Blood.

Hemoglobin Philly (beta 35 tyrosine phenylalanine): studies in the molecular pathology of hemoglobin.

F. Oski, J. Clegg, R. F. Rieder, 1969, The Journal of clinical investigation.

Selection and Common Monogenic Disease

J. Clegg, 2001 .

Haemoglobin Bart's in Saudi Arabia

M. Pembrey, J. Clegg, D. Weatherall, 1975, British journal of haematology.

Restriction endonuclease maps of the β‐like globin gene cluster in the British and Greek forms of HPFH, and for one example of Gγβ+ HPFH

R. W. Jones, J. Clegg, D. Weatherall, 1982 .

Restriction endonuclease maps of the beta-like globin gene cluster in the British and Greek forms of HPFH, and for one example of G gamma beta + HPFH.

R. W. Jones, J. Clegg, D. Weatherall, 1982, British journal of haematology.

Molecular basis of length polymorphism in the human zeta-globin gene complex.

S. Goodbourn, J. Clegg, D. Weatherall, 1983, Proceedings of the National Academy of Sciences of the United States of America.

Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring.

J. Clegg, D. Weatherall, S. Fucharoen, 1984, The Journal of clinical investigation.

Haemoglobin Constant Spring has an unstable α chain messenger RNA

J. Clegg, D. Weatherall, D. Higgs, 1982 .

Haemoglobin Icaria, a new chain-termination mutant which causes α thalassaemia

J. Clegg, D. Weatherall, I. CONTOPOLOU-GRIVA, 1974, Nature.

The molecular basis of alpha‐thalassaemia in Thailand.

S. Goodbourn, J. Clegg, D. Weatherall, 1984, The EMBO journal.

Gene conversions in the horse alpha-globin gene complex.

J. Clegg, 1987, Molecular biology and evolution.

Human globin gene analysis for a patient with beta-o/delta beta-thalassemia.

R. Williamson, J. Clegg, D. Weatherall, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Reduced soluble transferrin receptor concentrations in acute malaria in Vanuatu.

K. Maitland, T. Peto, J. Clegg, 1999, The American journal of tropical medicine and hygiene.

Switch from foetal to adult haemoglobin synthesis in normal and hypophysectomised sheep

J. Clegg, D. Weatherall, G. Dawes, 1976, Nature.

Localization of the horse (Equus caballus) alpha-globin gene complex to chromosome 13 by fluorescence in situ hybridization.

J. Clegg, E. Oakenfull, V. Buckle, 1993, Cytogenetics and cell genetics.

An Improved Method for the Characterization of Human Haemoglobin Mutants: Identification of α2β295GLU, Haemoglobin N (Baltimore)

J. Clegg, D. Weatherall, M. Naughton, 1965, Nature.

Phylogenetic relationships within the genus Equus and the evolution of alpha and theta globin genes.

J. Clegg, E. Oakenfull, 1998, Journal of molecular evolution.

Recombination Breakpoints in the Human β-Globin Gene Cluster

J. Kidd, J. Clegg, S. Thein, 1998 .

Thalassemia — a global public health problem

J. Clegg, D. Weatherall, 1996, Nature Medicine.

Polynesian origins and affinities: globin gene variants in eastern Polynesia.

A. Hill, J. Clegg, D. Weatherall, 1987, American journal of human genetics.

Molecular Analysis of the β-Globin Gene Cluster in the Niokholo Mandenka Population Reveals a Recent Origin of the βS Senegal Mutation

L. Excoffier, A. Langaney, R. Harding, 2002 .

and anAIuI Repeat

J. Clegg, D. Weatherall, D. Higgs, 2017 .

Severe malaria in children in Papua New Guinea.

J. Clegg, N. Alexander, S. Allen, 1996, QJM : monthly journal of the Association of Physicians.

Prevention of cerebral malaria in children in Papua New Guinea by southeast Asian ovalocytosis band 3.

M. Alpers, T. Peto, J. Clegg, 1999, The American journal of tropical medicine and hygiene.

High incidence of malaria in alpha-thalassaemic children.

C. Newbold, K. Maitland, T. Peto, 1996, Nature.

Molecular and population genetic analysis of allelic sequence diversity at the human beta-globin locus.

S. Fullerton, R. Harding, J. Clegg, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Evolutionary relationships of human populations from an analysis of nuclear DNA polymorphisms

A. Hill, J. Flint, J. Clegg, 1986, Nature.

Ahaptoglobinaemia in Melanesia: DNA and malarial antibody studies.

A. Hill, T. Peto, J. Clegg, 1987, Transactions of the Royal Society of Tropical Medicine and Hygiene.

Are we all out of Africa? (reply)

A. Hill, J. Clegg, S. Thein, 1986, Nature.

Evolutionary relationships of human populations

A. Hill, J. Clegg, S. Thein, 1986, Nature.

A population genetic survey of the haptoglobin polymorphism in Melanesians by DNA analysis.

A. Hill, J. Flint, S. Oppenheimer, 1986, American journal of human genetics.

Nucleic Acids Research

R. W. Jones, J. Clegg, D. Weatherall, 2010, Nucleic Acids Research.

Molecular basis of thalassaemia.

J. Clegg, D. Weatherall, 1976, British medical bulletin.

The synthesis of human haemoglobin A 2 during erythroid maturation.

J. Clegg, D. Weatherall, A. Roberts, 1972, Biochemical and biophysical research communications.

Is hemoglobin instability important in the interaction between hemoglobin E and beta thalassemia?

J. Clegg, D. Weatherall, D. Rees, 1998, Blood.

Interaction of five globin gene abnormalities in a Cambodian family

A. Hill, J. Clegg, D. Weatherall, 1986, British journal of haematology.

Born to clot: the European burden

M. Webster, J. Clegg, J. Guerreiro, 1999, British journal of haematology.

The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β‐Thalassaemia *

J. Clegg, D. Weatherall, S. Na-nakorn, 1969, British journal of haematology.

Isolation and characterization of DNA from archaeological bone

E. Hagelberg, J. Clegg, 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

The British type of non‐deletion HPFH: characterization of developmental changes in vivo and erythroid growth in vitro

J. Clegg, D. Weatherall, W. Wood, 1982, British journal of haematology.

High diversity of alpha-globin haplotypes in a Senegalese population, including many previously unreported variants.

L. Excoffier, A. Langaney, R. Harding, 1995, American journal of human genetics.

VNTR alleles associated with the alpha-globin locus are haplotype and population related.

J. Clegg, J. Martinson, A. J. Boyce, 1994, American journal of human genetics.

Allelic variation and linkage properties of a highly polymorphic restriction fragment in humans.

S. Goodbourn, J. Clegg, D. Weatherall, 1984, Molecular biology & medicine.

Alpha-thalassaemia caused by a polyadenylation signal mutation.

S. Goodbourn, J. Clegg, D. Weatherall, 1983, Nature.

THE CLINICAL AND MOLECULAR HETEROGENEITY OF THE THALASSEMIA SYNDROMES *

J. Clegg, D. Weatherall, D. Higgs, 1980, Annals of the New York Academy of Sciences.

Determination of Alpha Thalassaemia Phenotypes by Messenger RNA Analysis

D. Hunt, J. Clegg, D. Weatherall, 1980, British journal of haematology.

HLA class-I and class-II allele frequencies and two-locus haplotypes in Melanesians of Vanuatu and New Caledonia.

M. Barnardo, R. Harding, M. Bunce, 2004, Tissue antigens.

The molecular pathology of the ox globin genes

J. Clegg, D. Weatherall, D. Higgs, 2007 .

Structure and evolution of the horse zeta globin locus.

J. Flint, A. Taylor, J. Clegg, 1988, Journal of molecular biology.

Different hematologic phenotypes are associated with the leftward (-alpha 4.2) and rightward (-alpha 3.7) alpha+-thalassemia deletions.

A. Hill, S. Oppenheimer, J. Clegg, 1987, The Journal of clinical investigation.

Molecular Rearrangements of the Human α‐Globin Gene Cluster

A. Hill, S. Goodbourn, J. Clegg, 1985, Annals of the New York Academy of Sciences.

Melanesians and Polynesians share a unique alpha-thalassemia mutation.

A. Hill, S. Oppenheimer, J. Clegg, 1985, American journal of human genetics.

Interaction of the ααα globin gene haplotype and sickle haemoglobin

J. Clegg, D. Weatherall, D. Higgs, 1984 .

Association of two DNA polymorphisms in the alpha-globin gene cluster: implications for genetic analysis.

J. Clegg, D. Weatherall, D. Higgs, 1983, American journal of human genetics.

Thalassaemia intermedia in Cyprus: the interaction of alpha and beta thalassaemia.

J. Clegg, D. Weatherall, E. Kanavakis, 1983 .

Thalassaemia intermedia in Cyprus: the interaction of α and β thalassaemia

J. Clegg, D. Weatherall, D. Higgs, 1983, British journal of haematology.

α‐Globin gene deletions associated with Hb J Tongariki

J. Clegg, D. Weatherall, D. Higgs, 1982, British journal of haematology.

A NEW TRIPLICATED α‐GLOBIN GENE ARRANGEMENT IN MAN

J. Clegg, D. Weatherall, D. Higgs, 1981 .

HORSE HEMOGLOBIN POLYMORPHISM

J. Clegg, 1974, Annals of the New York Academy of Sciences.

Genetic disorders of human haemoglobin as models for analysing gene regulation.

J. Clegg, D. Weatherall, W. Wood, 1984, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The thalassaemia syndromes

J. B. Clegg, David J. Weatherall, J. Clegg, 1965 .

HEMOGLOBIN CONSTANT SPRING, AN UNUSUAL α‐CHAIN VARIANT INVOLVED IN THE ETIOLOGY OF HEMOGLOBIN H DISEASE

J. Clegg, D. Weatherall, 1974 .

Analysis of ancient bone DNA: techniques and applications.

Sheila J. Jones, E. Hagelberg, A. Boyde, 1991, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Thalassemia and malaria: new insights into an old problem.

J. Clegg, D. Weatherall, 1999, Proceedings of the Association of American Physicians.

THE CLINICAL AND CHEMICAL HETEROGENEITY OF THE β‐THALASSEMIAS

J. Clegg, D. Weatherall, A. Roberts, 1974, Annals of the New York Academy of Sciences.

Haemoglobin synthesis in human marrow maintained in tissue culture.

J. Clegg, D. Weatherall, W. Wood, 1971, British journal of haematology.

Amino-acid Replacements in Horse Haemoglobin

J. Kilmartin, J. Clegg, J. Clegg, 1967, Nature.

The population genetics of the haemoglobinopathies.

J. Flint, R. Harding, J. Clegg, 1993, Bailliere's clinical haematology.

Beta thalassemia in Melanesia: association with malaria and characterization of a common variant (IVS-1 nt 5 G----C).

A. Hill, J. Clegg, D. Weatherall, 1988, Blood.

High frequencies of α-thalassaemia are the result of natural selection by malaria

A. Hill, M. Alpers, J. Flint, 1986, Nature.

Esterases and a carbohydrate-splitting enzyme in the saliva of the cattle tick, Boophilus microplus.

J. Clegg, M. Naughton, A. Geczy, 1971, The Journal of parasitology.

Haemoglobin switching during development in normal and hypophysectomised fetal sheep.

J. Clegg, D. Weatherall, G. Dawes, 1977, Annales de recherches veterinaires. Annals of veterinary research.

Genetic organization of the polymorphic equine a globin locus and sequence of the Bll α1 gene

S. Goodbourn, J. Clegg, M. Braend, 1984 .

Comparison of theα-globin gene cluster structure in Perissodactyla

J. Flint, O. Ryder, J. Clegg, 2005, Journal of Molecular Evolution.

Novel alpha haemoglobin haplotypes in horses.

J. Flint, J. Clegg, A. Bowling, 2009, Animal genetics.

Determination of oxygen in semiconductor materials with a cryogenically pumped spark-source mass spectrometer

E. J. Millett, J. Clegg, I. Gale, 1973 .

The separation and isolation of the peptide chains of fibrin.

J. Clegg, K. Bailey, 1962, Biochimica et biophysica acta.

The computer evaluation and interpretation of photographically recorded spark source mass spectra

E. J. Millett, J. Clegg, J. A. Morice, 1974 .

Abnormal human haemoglobins

J. Clegg, D. Weatherall, M. Naughton, 1966 .

Hb A‐LIKE SICKLE HAEMOGLOBIN: Hb S‐PROVIDENCE

J. Clegg, E. Huehns, R. Gale, 1988, British journal of haematology.

The Negro Variety of Hereditary Persistence of Fetal Haemoglobin is a Mild Form of Thalassaemia

J. Clegg, D. Weatherall, S. Charache, 1976, British journal of haematology.

The Patterns of Fetal Haemoglobin Production in Leukaemia

W. McWhirter, J. Clegg, D. Weatherall, 1976, British journal of haematology.

K562 human leukaemic cells synthesise embryonic haemoglobin in response to haemin

J. Clegg, D. Weatherall, T. R. RUTHERFORD, 1979, Nature.

Haemoglobin synthesis during erythroid maturation in -thalassaemia.

J. Clegg, D. Weatherall, 1972, Nature: New biology.

ALPHA GLOBIN GENOTYPES IN TWO NORTH EUROPEAN POPULATIONS

A. Hill, J. Flint, J. Clegg, 1986, British journal of haematology.

Independent recombination events between the duplicated human alpha globin genes; implications for their concerted evolution.

A. Hill, J. Clegg, D. Weatherall, 1984, Nucleic acids research.

Interaction of heterocellular hereditary persistence of foetal haemoglobin with β thalassaemia and sickle cell anaemia

J. Clegg, D. Weatherall, W. Wood, 1976, Nature.

Benign sickle-cell anaemia.

J. Clegg, D. Weatherall, M. J. Brown, 1972, The Lancet.

Linkage analysis of nondeletion hereditary persistence of fetal hemoglobin.

J. Clegg, D. Weatherall, H. Ayyub, 1982, Science.

A MODEL FOR THE PERSISTENCE OR REACTIVATION OF FETAL HÆMOGLOBIN PRODUCTION

J. Clegg, D. Weatherall, W. Wood, 1976, The Lancet.

Linkage relationships between beta- and delta-structural loci and African forms of beta thalassaemia.

J. Clegg, D. Weatherall, P. Milner, 1976, Journal of medical genetics.

A Form of Hereditary Persistence of Fetal Haemoglobin Characterized by Uneven Cellular Distribution of Haemoglobin F and the Production of Haemoglobins A and A2 in Homozygotes

J. Clegg, W. Wood, D. Weatherall, 1975, British journal of haematology.

Thalassaemia in the British

M. Pembrey, J. Clegg, D. Weatherall, 1973, British medical journal.

A new genetic basis for hemoglobin-H disease.

M. Pembrey, J. Clegg, D. Weatherall, 1980, The New England journal of medicine.

The interaction of alpha-thalassemia and homozygous sickle-cell disease.

J. Clegg, D. Weatherall, D. Higgs, 1982, The New England journal of medicine.

Why are some genetic diseases common?

J. Flint, A. Boyce, R. Harding, 1993, Human Genetics.

Genetic and Molecular Analysis of Mild Forms of Homozygous β‐Thalassemia

J. Clegg, D. Weatherall, D. Higgs, 1985 .

MOLECULAR BASIS FOR MILD FORMS OF HOMOZYGOUS BETA-THALASSAEMIA

J. Clegg, D. Weatherall, D. Higgs, 1981, The Lancet.

A novel α-globin gene arrangement in man

J. Clegg, D. Weatherall, D. Higgs, 1980, Nature.

Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

J. Clegg, W. Wood, T. Huisman, 1977, American journal of human genetics.

Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok).

J. Clegg, M. Naughton, D. J. Weatherball, 1966, Journal of molecular biology.

Recent developments in the molecular genetics of human hemoglobin

D. J. Weatherall, J. B. Clegg, J. Clegg, 1979, Cell.

Homozygous beta thalassaemia in Liberia.

J. Clegg, D. Weatherall, M. Willcox, 1975, Journal of medical genetics.

HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN

J. Clegg, D. Weatherall, 1975, British journal of haematology.

Homozygous β thalassaemia in Liberia.

J. Clegg, D. Weatherall, M. Willcox, 1975 .

Occurrence of Gγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia

J. Clegg, D. Weatherall, C. Kattamis, 1979 .

Human globin gene expression: Control of β, δ and δβ chain production

J. Clegg, D. Weatherall, W. Wood, 1978, Cell.

G gamma delta beta thalassaemia and g gamma HPFH (Hb Kenya type): comparison of 2 new cases.

J. Clegg, D. Weatherall, W. Wood, 1977, Journal of medical genetics.

Molecular Basis of Thalassaemia

J. Clegg, D. Weatherall, 1975 .

Preliminary surveys for the prevalence of the thalassemia genes in some African populations.

J. Clegg, D. Weatherall, H. Gilles, 1971, Annals of tropical medicine and parasitology.

alpha+-Thalassemia protects children against disease caused by other infections as well as malaria.

M. Alpers, T. Peto, J. Clegg, 1997, Proceedings of the National Academy of Sciences of the United States of America.

The molecular basis for beta o thalassaemia intermedia in an Iranian individual.

J. Clegg, D. Weatherall, R. Trent, 1982, British journal of haematology.

α-Thalassaemia caused by a polyadenylation signal mutation

S. Goodbourn, J. Clegg, D. Weatherall, 1983, Nature.

THE SIGNIFICANCE OF HAEMOGLOBIN H IN PATIENTS WITH MENTAL RETARDATION OR MYELOPROLIFERATIVE DISEASE

J. Clegg, D. Weatherall, W. Wood, 1982, British Journal of Haematology.

The Genetic Basis of Hb Q‐H Disease

J. Clegg, D. Weatherall, D. Higgs, 1980, British journal of haematology.

Embryonic erythroid differentiation in the human leukemic cell line K562.

R. W. Jones, D J Weatherall, J. Clegg, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Antenatal diagnosis of thalassaemia major.

J. Clegg, D. Weatherall, B. Alter, 1978, British medical journal.

Globin Synthesis in Thalassaemia: An in vitro Study

J. Clegg, D. Weatherall, M. Naughton, 1965, Nature.

Developmental biology of human hemoglobins.

J. Clegg, D. Weatherall, W. Wood, 2016, Progress in hematology.

Maternal synthesis of haemoglobin F in pregnancy.

M. Pembrey, J. Clegg, D. Weatherall, 1973, Lancet.

Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow.

J. Clegg, D. Weatherall, G. Chalevelakis, 1975, Proceedings of the National Academy of Sciences of the United States of America.

Why are hemoglobin F levels increased in HbE/beta thalassemia?

J. Clegg, D. Weatherall, D. Rees, 1999, Blood.

The interaction between Plasmodium falciparum and P. vivax in children on Espiritu Santo island, Vanuatu.

C. Newbold, K. Maitland, T. Peto, 1996, Transactions of the Royal Society of Tropical Medicine and Hygiene.

High incidence of malaria in α-thalassaemic children

C. Newbold, K. Maitland, T. Peto, 1996, Nature.

Genetic disorders of hemoglobin.

J. Clegg, D. Weatherall, 1999, Seminars in hematology.

Prenatal diagnosis of the common haemoglobin disorders.

J. Clegg, D. Weatherall, S. Thein, 1985, Journal of medical genetics.

Molecular basis for dominantly inherited inclusion body beta-thalassemia.

J. Clegg, D. Weatherall, S. Thein, 1990, Proceedings of the National Academy of Sciences of the United States of America.

G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.

J. Clegg, D. Weatherall, D. Higgs, 1979, Journal of medical genetics.

Rapid postsynthetic destruction of unstable haemoglobin Bushwick

J. Clegg, R. F. Rieder, D. Wolf, 1975, Nature.

y 6 ip thalassaemia and G-HPFH ( Hb Kenya type ) Comparison of 2 new cases

J. Clegg, D. Weatherall, W. Wood, 2022 .

Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene.

D. Hunt, J. Clegg, D. Weatherall, 1979, Lancet.

A direct estimate of the number of human γ-globin genes

R. Williamson, J. Clegg, D. Weatherall, 1976, Cell.

A Comparison of the Homozygous States for Gγ and GγAγδβ Thalassaemia

J. Clegg, D. Weatherall, J. White, 1979 .

A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemia.

J. Clegg, D. Weatherall, W. Wood, 1979, British journal of haematology.

Hereditary Persistence of Foetal Haemoglobin associated with a γβ Fusion Variant, Haemoglobin Kenya

J. Clegg, D. Weatherall, H. Gilles, 1973 .

Haemoglobin F(Malta): a New Foetal Haemoglobin Variant with a High Incidence in Maltese Infants

J. Clegg, D. Weatherall, M. Cauchi, 1969, Nature.

Defective synthesis of HbE is due to reduced levels of βE mRNA

J. Clegg, D. Weatherall, W. Wood, 1980, Nature.

The Clinical and Biosynthetic Characterization of αβ‐Thalassaemia

J. Clegg, D. Weatherall, H. Knox-macaulay, 1972, British journal of haematology.

The thalassaemias.

J. Clegg, D. Weatherall, 2008, The Medical journal of Australia.

Globin Synthesis in Normal Human Bone Marrow

J. Clegg, D. Weatherall, G. Chalevelakis, 1976, British journal of haematology.

Synthesis in vitro of anti-Lepore haemoglobin.

J. Clegg, D. Weatherall, Y. Ohta, 1973, Nature: New biology.

Haemoglobin synthesis in human bone marrow culture.

J. Clegg, D. Weatherall, W. Wood, 1972, Biochimica et biophysica acta.

EMBRYONIC HEMOGLOBIN SYNTHESIS IN HUMAN ERYTHROLEUKEMIA CELLS *

J. Clegg, D. Weatherall, T. Rutherford, 1980, Annals of the New York Academy of Sciences.

Molecular genetics of human hemoglobin.

J. Clegg, D. Weatherall, 1976, Annual review of genetics.

Proceedings: Hb Kenya: a clue to the genetic control of human foetal haemoglobin synthesis.

J. Clegg, D. Weatherall, D. Smith, 1974, British journal of haematology.

Proceedings: The translation of human globin messenger RNA in heterologous assay systems.

J. Clegg, D. Weatherall, J. Pritchard, 1974, British journal of haematology.

Identification of slow-moving haemoglobins in haemoglobin H disease from different racial groups.

J. Clegg, D. Weatherall, P. Fessas, 1972, Lancet.

Molecular Defect of β Thalassaemia

J. Clegg, 1971, Nature.

Haemoglobin Synthesis in β-Thalassaemia

J. Clegg, D. Weatherall, S. Na-nakorn, 1968, Nature.

Molecular basis for acquired haemoglobin H disease

J. Clegg, D. Weatherall, J. Old, 1977, Nature.

Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.

J. Clegg, D. Weatherall, C. Beresford, 1972, Journal of medical genetics.

Haemoglobin Ocho Rios ( beta52 (D3) aspartic acid leads to alanine): a new beta-chain variant of haemoglobin A found in combination with haemoglobin S.

J. Clegg, D. Weatherall, J. Weatherall, 1972, Journal of medical genetics.

DISORDERED GLOBIN SYNTHESIS IN THALASSEMIA

J. Clegg, D. Weatherall, 1969, Annals of the New York Academy of Sciences.

NEGRO α-THALASSÆMIA IS CAUSED BY DELETION OF A SINGLE α-GLOBIN GENE

D. Hunt, J. Clegg, D. Weatherall, 1979, The Lancet.

Historical Perspectives: The Many and Diverse Routes to Our Current Understanding of the Thalassaemias

J. Clegg, D. Weatherall, 2008 .

Characterisation of a new α thalassemia 1 defect due to a partial deletion of the α globin gene complex

J. Clegg, D. Higgs, L. Pressley, 1980 .

Defective synthesis of HbE is due to reduced levels of beta E mRNA.

J. Clegg, D. Weatherall, W. Wood, 1980, Nature.

Aplastic anemia with fetallike erythropoiesis following androgen therapy.

J. Clegg, A. Brown, W. Marsh, 1978, Blood.

The Molecular Pathology of the Thalassaemias

J. Clegg, D. Weatherall, 2008 .

Restriction mapping of a new deletion responsible for G gamma (delta beta)o thalassemia.

R. W. Jones, J. Clegg, D. Weatherall, 1981, Nucleic acids research.

A novel rearrangement of the human beta-like globin gene cluster.

J. Clegg, D. Weatherall, D. Bowden, 1981, Nucleic acids research.

Separation of the alpha and beta-chains of human hemoglobin.

J. Clegg, D. Weatherall, M. Naughton, 1968, Nature.

Genetic and molecular diversity in nondeletion Hb H disease.

J. Clegg, D. Weatherall, D. Higgs, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Haemoglobin-H disease due to a unique haemoglobin variant with an elongated alpha-chain.

J. Clegg, D. Weatherall, P. Milner, 1971, Lancet.

Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis

J. Clegg, D. Weatherall, W. Wood, 1978, British journal of haematology.

HÆMOGLOBIN-H DISEASE DUE TO A UNIQUE HÆMOGLOBIN VARIANT WITH AN ELONGATED α-CHAIN

J. Clegg, D. Weatherall, P. Milner, 1971 .

Themolecular basis ofoa-thalassaemia inThailand

S. Goodbourn, J. Clegg, D. Weatherall, 1984 .

INADEQUACY OF Hb BART'S AS AN INDICATOR OF α THALASSAEMIA

J. Clegg, D. Weatherall, D. Higgs, 1982, British journal of haematology.

The Laboratory Diagnosis of the Thalassaemias

J. Clegg, D. Weatherall, 2008 .

Simultaneous expression of globin genes for embryonic and adult hemoglobins during mammalian ontogeny.

J. Clegg, J. Bertles, T. Boussios, 1982, Science.

HB F-Granada or α2Gγ222 (B4)ASP→VAL: A New Human Fetal Hemoglobin Variant

J. Clegg, J. M. Pablos, 1988 .

Screening procedures for quantitative abnormalities in hemoglobin synthesis.

J. Clegg, D. Weatherall, 1981, Methods in enzymology.

Archaic African and Asian lineages in the genetic ancestry of modern humans.

R. Griffiths, S. Fullerton, J. Bond, 1997, American journal of human genetics.

Molecular and population genetic analysis of allelic sequence diversity at the human beta-globin locus.

S. Fullerton, R. Harding, J. Clegg, 1994, Proceedings of the National Academy of Sciences of the United States of America.

Evidence for mitochondrial DNA recombination in a human population of island Melanesia

E. Hagelberg, P. Lio’, S. Whelan, 1999, Proceedings of the Royal Society of London. Series B: Biological Sciences.

Polymerase chain reaction protocols for alpha globin haplotype polymorphisms

J. Clegg, J. Martinson, K. L. Miles, 2001, British journal of haematology.

α‐Thalassaemia and globin gene rearrangements in French Polynesia

J. Roux, J. Clegg, J. Martinson, 1995, European journal of haematology.

Non-deletion haemoglobin H disease in Papua New Guinea.

A. Hill, J. Clegg, D. Weatherall, 1987, Journal of medical genetics.

The evolution of tandemly repetitive DNA: recombination rules.

R. Harding, J. Clegg, A. J. Boyce, 1992, Genetics.

Characterization of β-globin mRNA in the β0 thalassemias

J. Clegg, D. Weatherall, N. Proudfoot, 1978, Cell.

Coincidence and protein structure.

J. Clegg, J WILLIAMS, J B CLEGG, 1961, Journal of molecular biology.

Assay of Thalassaemic Messenger RNA in the Wheat Germ System

J. Clegg, D. Weatherall, J. Pritchard, 1976, British journal of haematology.

The Molecular Defect in Thalassaemia

J. Clegg, 1976 .

Haemoglobin J Tongariki is associated with α thalassaemia

J. Clegg, D. Weatherall, J. Old, 1978, Nature.

Haemoglobin Constant Spring—A Chain Termination Mutant ?

J. Clegg, D. Weatherall, P. Milner, 1971, Nature.

Phylogenetic Relationships Within the Genus Equus and the Evolution of α and θ Globin Genes

J. Clegg, E. Oakenfull, Oakenfull Ea, 1998, Journal of Molecular Evolution.

A mouse beta-globin mutant that is an exact model of hemoglobin Rainier in man.

J. Clegg, J. Peters, J. Loutit, 1985, Genetics.

Thalassaemia in Vanuatu, South‐West Pacific: frequency and haematological phenotypes of young children

K. Maitland, J. Clegg, D. Weatherall, 1995, British journal of haematology.

Demographic reductions and genetic bottlenecks in humans: minisatellite allele distributions in oceania

R. Harding, J. Clegg, J. Martinson, 1993, Human Genetics.

Population bottlenecks in Polynesia revealed by minisatellites

J. Flint, J. Clegg, J. Martinson, 1989, Human Genetics.

Recombination breakpoints in the human beta-globin gene cluster.

J. Kidd, J. Clegg, S. Thein, 1998, Blood.

Direct cloning of specific genomic DNA sequences in plasmid libraries following fragment enrichment.

A. Hill, J. Clegg, D. Higgs, 1985, Nucleic acids research.

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation.

J. Clegg, D. Rees, Y. T. Liu, 1998, American journal of human genetics.

Detection of the Factor V Leiden Mutation Using Whole Blood PCR

J. Clegg, D. Rees, M. Cox, 1996, Thrombosis and Haemostasis.

Polycythemia associated with a hemoglobinopathy.

J. Clegg, D. Weatherall, S. Charache, 1966, The Journal of clinical investigation.

Haemoglobin Synthesis in α-Thalassaemia (Haemoglobin H Disease)

J. Clegg, D. Weatherall, D. Weatherall, 1967, Nature.

Two New Haemoglobin Variants involving Proline Substitutions

J. Clegg, D. Weatherall, W. H. Boon, 1969, Nature.

Alpha-globin gene haplotypes in South American Indians.

J. Clegg, M. Zago, J. Guerreiro, 1995, Human biology.

THE MOLECULAR BASIS FOR β° THALASSAEMIA INTERMEDIA IN AN IRANIAN INDIVIDUAL

J. Clegg, D. Weatherall, E. R. Huehns, 1982 .

The alpha-chain-termination mutants and their relation to the alpha-thalassaemias.

J. Clegg, D. Weatherall, 1975, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Homozygous state for Hb Constant Spring (slow-moving Hb X components).

J. Clegg, D. Weatherall, L. Lie-injo, 1974, Blood.

Separation of the α and β-Chains of Human Haemoglobin

J. Clegg, D. Weatherall, M. Naughton, 1968, Nature.

δβ‐Thalassaemia in a Chinese Family

J. Clegg, D. Weatherall, W. Wood, 1972 .

The thalassaemia syndromes. 2nd Edition.

J. Clegg, D. Weatherall, 1972 .

Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management

J. Farrar, T. Peto, J. Clegg, 2010, British journal of haematology.

A novel silent posttranslational mechanism converts methionine to aspartate in hemoglobin Bristol (beta 67[E11] Val-Met->Asp).

J. Clegg, B. Green, J. Rochette, 1996, Blood.

Alkaline transfer of small restriction fragments from polyacrylamide gels.

J. Clegg, J. Martinson, 1990, Nucleic acids research.

THE STRUCTURAL ANALYSIS OF THE HUMAN EPSILON‐GLOBIN GENE AND ITS PRODUCT

J. Clegg, N. Proudfoot, Francisco E. Baralle, 1980, Annals of the New York Academy of Sciences.

Hemoglobin polymorphism in Equus przewalskii and E. caballus analyzed by isoelectric focusing.

O. Ryder, J. Clegg, R. Sparkes, 1979, Comparative biochemistry and physiology. B, Comparative biochemistry.

Genetic polymorphisms in prehistoric Pacific islanders determined by analysis of ancient bone DNA

E. Hagelberg, J. Clegg, 1993, Proceedings of the Royal Society of London. Series B: Biological Sciences.

A gene tree for β-globin sequences from melanesia

R. Griffiths, S. Fullerton, R. Harding, 2009, Journal of Molecular Evolution.

Analysis of variation in the human beta-globin gene cluster using a novel DHPLC technique.

M. Webster, J. Clegg, R. Wells, 2002, Mutation research.

Polymorphism and Divergence in the β-Globin Replication Origin Initiation Region

S. Fullerton, J. Bond, R. Harding, 2000 .

(Aγδβ)° thalassaemia: similarity of phenotype in four different molecular defects, including one newly described

R. W. Jones, J. Clegg, D. Weatherall, 1984, British journal of haematology.

alpha thalassemia in black populations.

J. Clegg, D. Weatherall, D. Higgs, 1980, The Johns Hopkins medical journal.

The molecular basis of hemoglobin Grady.

A. F. Scott, J. Clegg, H. Kazazian, 1981, American journal of human genetics.

5-AZACYTIDINE FOR BETA-THALASSAEMIA?

W. Bodmer, J. Clegg, D. Weatherall, 1983, The Lancet.

Common 5′ β-globin RFLP haplotypes harbour a surprising level of ancestral sequence mosaicism

M. Webster, R. Harding, J. Clegg, 2003, Human Genetics.

Thalassemia Revisited

J. Clegg, D. Weatherall, 1982, Cell.

Major rearrangement in the human beta-globin gene cluster.

R. W. Jones, J. Clegg, D. Weatherall, 1981, Nature.

An ancient common origin of aboriginal Australians and New Guinea highlanders is supported by alpha-globin haplotype analysis.

R. Harding, J. Clegg, J. Martinson, 1996, American journal of human genetics.

Haemoglobin Radcliffe (α2β299(G1)Ala): A High Oxygen‐Affinity Variant Causing Familial Polycythaemia

M. Perutz, J. Clegg, D. Weatherall, 1977 .

Evidence for a single origin of factor V Leiden

J. Clegg, J. Martinson, M. Cox, 1996, British journal of haematology.

Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency.

H. Simmonds, J. Clegg, D. Weatherall, 1996, Blood.

Analysis ofthehumana-globin genecluster reveals ahighly informative genetic locus

A. Hill, J. Flint, J. Clegg, 1986 .

Red blood cell phenotypes in the α+ thalassaemias from early childhood to maturity

K. Maitland, J. Clegg, D. Weatherall, 1996, British journal of haematology.

Hemoglobin Constant Spring, and unusual alpha-chain variant involved in the etiology of hemoglobin H disease.

J. Clegg, D. Weatherall, 1974, Annals of the New York Academy of Sciences.

Haemoglobin Constant Spring has an unstable alpha chain messenger RNA.

D. Hunt, J. Clegg, D. Weatherall, 1982, British journal of haematology.

Heterogeneity and origins of the alpha-thalassemias.

J. Clegg, D. Weatherall, D. Higgs, 1987, Birth defects original article series.

Genetic disorders of haemoglobin

J. Clegg, D. Weatherall, 2000 .

The β and δβ Thalassaemias in Association with Structural Haemoglobin Variants

J. Clegg, D. Weatherall, 2008 .

The molecular pathology of the alpha globin genes.

J. Clegg, D. Weatherall, D. Higgs, 1988, The British journal of cancer. Supplement.

Immunoglobulin λ-chains. The complete amino acid sequence of a Bence-Jones protein

J. Clegg, J. Jarvis, C. Milstein, 1968 .

Southeast Asian ovalocytosis and pregnancy in a malaria-endemic region of Papua New Guinea.

J. Clegg, D. Weatherall, S. Allen, 2007, The American journal of tropical medicine and hygiene.

The population genetics of the haemoglobinopathies.

J. Flint, R. Harding, J. Clegg, 1998, Bailliere's clinical haematology.

Horse haemoglobin polymorphism: evidence for two linked non-allelic α-chain genes

J. Clegg, 1970, Proceedings of the Royal Society of London. Series B. Biological Sciences.

Molecular population genetic studies of the island peoples of the South Pacific

R. Harding, J. Clegg, 1996, American journal of human biology : the official journal of the Human Biology Council.

REPORT : SOUTHEAST ASIAN OVALOCYTOSIS AND PREGNANCY IN A MALARIA-ENDEMIC REGION OF PAPUA NEW GUINEA

J. Clegg, D. Weatherall, S. Allen, 2007 .

SHORT REPORT: SOUTHEAST ASIAN OVALOCYTOSIS AND PREGNANCY IN A MALARIA-ENDEMIC REGION OF PAPUA NEW GUINEA

J. Clegg, D. Weatherall, S. Allen, 2007 .

Haemoglobin Icaria, a new chain-termination mutant with causes alpha thalassaemia.

J. Clegg, D. Weatherall, I. CONTOPOLOU-GRIVA, 1974, Nature.

Minisatellite mutational processes reduce Fst estimates

L. Excoffier, M. Beaumont, J. Flint, 1999, Human Genetics.

Rapid detection of α‐thalassaemia deletions and α‐globin gene triplication by multiplex polymerase chain reactions

J. Clegg, D. Weatherall, C. Fisher, 2000, British journal of haematology.

High frequency of beta thalassaemia in a small island population in Melanesia.

A. Hill, J. Clegg, D. Weatherall, 1987, Journal of medical genetics.

β‐Globin polymorphisms in amerindian populations from the brazilian amazon

J. Clegg, D. Meyer, J. Guerreiro, 2012, American journal of human biology : the official journal of the Human Biology Council.

Embryonic hemoglobin: sequence of the epsilon and zeta chains.

J. Clegg, 1980, Texas reports on biology and medicine.

Hpal, HindIII, and BamHI polymorphisms 3′ of the human β‐globin gene can be detected by a single polymerase chain reaction amplification product

S. Fullerton, J. Clegg, 1994, American journal of hematology.

DNA from ancient Easter Islanders

E. Hagelberg, J. Clegg, D. Turbón, 1994, Nature.

Polymorphism and divergence in the beta-globin replication origin initiation region.

S. Fullerton, J. Bond, R. Harding, 2000, Molecular biology and evolution.

Evidence for mitochondrial DNA recombination in a human population of island Melanesia: correction

E. Hagelberg, S. Whelan, J. Clegg, 2000, Proceedings of the Royal Society of London. Series B: Biological Sciences.

The developmental genetics of human hemoglobin.

R. W. Jones, J. Clegg, D. Weatherall, 1985, Progress in clinical and biological research.

Alpha thalassaemia is associated with increased soluble transferrin receptor levels

J. Clegg, D. Weatherall, K. Maitland, 1998, British journal of haematology.

RELATIVE ROLES OF GENETIC FACTORS, DIETARY DEFICIENCY, AND INFECTION IN ANAEMIA IN VANUATU, SOUTH-WEST PACIFIC

A. Hill, J. Clegg, D. Weatherall, 1985, The Lancet.

Large scale screening for haemoglobin disorders in southern Vietnam: implications for avoidance and management

J. Farrar, T. Peto, J. Clegg, 2010, British journal of haematology.

Alpha-thalassaemia and the malaria hypothesis.

A. Hill, J. Flint, J. Clegg, 1987, Acta haematologica.

Molecular Analysis of the β-Globin Gene Cluster in the Niokholo Mandenka Population Reveals a Recent Origin of the βS Senegal Mutation

L. Excoffier, A. Langaney, R. Harding, 2002 .

Rugged Thin Film Diode Liquid Crystal Switches Based on Amorphous Sin x :H

J. N. Sandoe, J. Clegg, J. Shannon, 1997 .