W. Wood

发表

A Regulatory SNP Causes a Human Genetic Disease by Creating a New Transcriptional Promoter

Vip Viprakasit, Jan-Fang Cheng, Edward M. Rubin, 2006, Science.

Association between active genes occurs at nuclear speckles and is modulated by chromatin environment

F. Iborra, J. Hughes, D. Higgs, 2008, The Journal of cell biology.

Deletion of the mouse alpha-globin regulatory element (HS -26) has an unexpectedly mild phenotype.

D. Higgs, J. Sharpe, J. Sloane-Stanley, 2002, Blood.

Genetic dissection of the α-globin super-enhancer in vivo

L. Pennacchio, J. Telenius, J. Hughes, 2016, Nature Genetics.

Nprl3 is required for normal development of the cardiovascular system

Monika S. Kowalczyk, C. Ponting, S. Bhattacharya, 2012, Mammalian Genome.

Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model.

P. Nolan, D. Higgs, J. Sharpe, 2007, American journal of human genetics.

Loss of Atrx Affects Trophoblast Development and the Pattern of X-Inactivation in Extraembryonic Tissues

D. Higgs, J. Sharpe, R. Gibbons, 2006, PLoS genetics.

Understanding alpha globin gene expression: a step towards effective gene therapy.

D. Higgs, J. Sharpe, W. Wood, 1998, Seminars in hematology.

Haemoglobin Bart's hydrops syndrome in Greece.

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

δβ-Thalassemia is due to a gene deletion

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

The British form of hereditary persistence of fetal hemoglobin results from a single base mutation adjacent to an S1 hypersensitive site 5' to the A gamma globin gene.

D. Weatherall, W. Wood, V. Tate, 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 .

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

C. Langford, D. Higgs, H. Ayyub, 2003, Nature Genetics.

HAEMOGLOBIN PRODUCTION DURING DEVELOPMENT

W. Wood, 1981 .

The complexities of beta globin gene regulation.

W. Wood, 1996, Trends in genetics : TIG.

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

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

Healing of broken human chromosomes by the addition of telomeric repeats.

H. Williams, D. Higgs, H. Ayyub, 1994, American journal of human genetics.

A Novel Deletion in the β‐Globin Gene Complex

D. Weatherall, E. Kanavakis, S. Thein, 1985, Annals of the New York Academy of Sciences.

Disorders of Hemoglobin: The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin

S. Thein, W. Wood, 2009 .

Global gene expression analysis of human erythroid progenitors.

A. Nandi, S. McGowan, D. Higgs, 2011, Blood.

De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).

J. Lamb, A. Wilkie, D. Higgs, 1993, American journal of human genetics.

β + Thalassaemia—Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia

W. Wood, J. Wainscoat, G. Tamagnini, 1983 .

heterogeneity in congenital dyserythropoietic anemia type I gene reveals genetic CDAN1 Linkage and mutational analysis of the

P. Vyas, D. Higgs, H. Tamary, 2011 .

Linkage and mutational analysis of the CDAN1 gene reveals genetic heterogeneity in congenital dyserythropoietic anemia type I.

P. Vyas, D. Higgs, H. Tamary, 2006, Blood.

We Also Investigated 6 Sporadic Cases with Cda I for Cdan1

H. Tamary, W. Wood, N. Avidan, 2006 .

Severe intrauterine anemia: a new form of ɛγγδβ thalassemia presenting in utero in a Norwegian family

N. Roberts, C. Fisher, W. Wood, 2009, Haematologica.

Genetic control of F cells in human adults.

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

Bb1‐3, a transgenic hybrid cell line with erythroid and megakaryocytic differentiation potential that expresses high levels of human γ‐globin and human β‐globin

A. Thomson, N. Roberts, W. Wood, 1998 .

Foetal erythropoiesis in human leukaemia

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

A novel deletion causing alpha thalassemia clarifies the importance of the major human alpha globin regulatory element.

D. Higgs, V. Viprakasit, H. Ayyub, 2006, Blood.

The congenital dyserythropoietic anemias.

W. Wood, R. Renella, 2009, Hematology/oncology clinics of North America.

Advances in the understanding of the congenital dyserythropoietic anaemias

W. Wood, S. Wickramasinghe, 2005, British journal of haematology.

Analysis of a 70 kb segment of DNA containing the human zeta and alpha-globin genes linked to their regulatory element (HS-40) in transgenic mice.

D. Higgs, J. Sharpe, W. Wood, 1994, Nucleic acids research.

7 Increased HbF in adult life

W. Wood, 1993 .

Post‐natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parental Hb F levels

W. Wood, G. Serjeant, R. Hayes, 1982, British journal of haematology.

Control of haemoglobin switching by a developmental clock?

W. Wood, G. Breckon, C. Bunch, 1985, Nature.

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.

Hematologic and biosynthetic studies in homozygous hemoglobin Constant Spring.

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

Haemoglobin Synthesis in Human Erythroid Bursts during Ontogeny: Reproducibility and Sensitivity to Culture Conditions

J. Adamson, D. Weatherall, W. Wood, 1981, British journal of haematology.

Clinical features and molecular analysis of acquired hemoglobin H disease.

D. Weatherall, D. Higgs, W. Wood, 1983, The American journal of medicine.

Haemopoietic progenitor cell lines generated by the myeloproliferative leukaemia virus: a model system to analyse murine and human lineage‐affiliated genes

A. Thomson, N. Roberts, W. Wood, 1999, British journal of haematology.

Haemoglobin synthesis during human foetal development.

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

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

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

A single beta-globin locus control region element (5' hypersensitive site 2) is sufficient for developmental regulation of human globin genes in transgenic mice

J. Sharpe, C. Abbott, W. Wood, 1992, Molecular and cellular biology.

Increased HbF in adult life.

W. Wood, 1993, Bailliere's clinical haematology.

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.

Homozygous G γλβ thalassaemia

W. Wood, J. Wood, J. Matthews, 1981 .

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.

Genetic complexity in sickle cell disease

D. Higgs, W. Wood, Douglas R. Higgs, 2008, Proceedings of the National 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.

Haemoglobin synthesis in human marrow maintained in tissue culture.

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

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.

PATTERN OF MATERNAL F-CELL PRODUCTION DURING PREGNANCY

D. Weatherall, W. Wood, A. Turnbull, 1977, The Lancet.

The interaction of α thalassaemia with heterozygous β thalassaemia

D. Weatherall, E. Kanavakis, W. Wood, 1982, British journal of haematology.

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

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

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.

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.

CELLULAR ORIGINS OF THE FETAL-HÆMOGLOBIN-CONTAINING CELLS OF NORMAL ADULTS

J. Adamson, D. Weatherall, W. Wood, 1979, The Lancet.

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

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

The triplicated α gene locus and β thalassaemia

W. Wood, J. Wainscoat, C. Kattamis, 1983 .

The triplicated alpha gene locus and beta thalassaemia.

E. Kanavakis, W. Wood, J. Wainscoat, 1983, British journal of haematology.

MOLECULAR BASIS FOR MILD FORMS OF HOMOZYGOUS BETA-THALASSAEMIA

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

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.

Hematologic Changes and Hemoglobin Analysis in β Thalassemia Heterozygotes during the First Year of Life

D. Weatherall, M. Bennett, W. Wood, 1982, Pediatric Research.

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.

y 6ip thalassaemia andG-HPFH (HbKenyatype) Comparison of2new cases

W. Wood, H. Gyde, D. Obeid, 1977 .

Developmental genetics of the human haemoglobins.

D. Weatherall, W. Wood, 1983, The Biochemical journal.

Erythroid differentiation in CGL cells from a patient with blast crisis.

D. Weatherall, V. Buckle, W. Wood, 1984, Leukemia research.

Fetal-to-adult hemopoietic cell transplantation: is hemoglobin synthesis gestational age-dependent?

W. Wood, C. Bunch, 1983, Progress in clinical and biological research.

Antenatal diagnosis of thalassaemia major.

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

Developmental biology of human hemoglobins.

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

A novel molecular basis for beta thalassemia intermedia poses new questions about its pathophysiology.

D. Weatherall, J. Sloane-Stanley, N. Olivieri, 2005, Blood.

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.

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

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

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.

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

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

Haemoglobin synthesis in human bone marrow culture.

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

Sickle beta 0 thalassemia in Eastern Saudi Arabia.

M. Pembrey, D. Weatherall, W. Wood, 1980, American journal of human genetics.

Gene expression in somatic cell hybrids derived from embryonic mice transgenic for human globin genes

N. Roberts, J. Sharpe, W. Wood, 1996, British journal of haematology.

The Molecular Pathology of the Thalassaemias

S. Thein, W. Wood, Higgs, 2008 .

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

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

Erythroid Cell Proliferation in Human Bone Marrow Suspension Cultures

W. Wood, 1974, British journal of haematology.

Foetal haemoglobin in patients with thyroid disorders.

P. D. Bewsher, W. Wood, R. Davidson, 2009, Scandinavian journal of haematology.

Regulation of human fetal and adult globin genes in mouse erythroleukemia cells.

C. Abbott, W. Wood, B. J. Morley, 1991, Blood.

Beta-thalassemia unlinked to the beta-globin gene in an English family.

S. Thein, W. Wood, S. Wickramasinghe, 1993, Blood.

Long-range regulation of α globin gene expression during erythropoiesis

D. Higgs, W. Wood, 2008, Current opinion in hematology.

Long‐range chromosomal interactions regulate the timing of the transition between poised and active gene expression

D. Higgs, J. Sloane-Stanley, D. Vernimmen, 2007 .

Long-range chromosomal interactions regulate the timing of the transition between poised and active gene expression.

Douglas R Higgs, D. Higgs, J. Sloane-Stanley, 2007, The EMBO journal.

Intragenic enhancers act as alternative promoters.

Monika S. Kowalczyk, Thomas A Milne, Douglas R Higgs, 2012, Molecular cell.

Manipulating the Mouse Genome to Engineer Precise Functional Syntenic Replacements with Human Sequence

J. Hughes, D. Higgs, J. Sharpe, 2007, Cell.

Coregulated human globin genes are frequently in spatial proximity when active

Veronica J. Buckle, Ann Atzberger, Francisco J. Iborra, 2006, The Journal of cell biology.

A human PKD1 transgene generates functional polycystin-1 in mice and is associated with a cystic phenotype.

J. Sharpe, J. Sloane-Stanley, L. Strmečki, 2000, Human molecular genetics.

A lack of border guards

D. Higgs, W. Wood, 2006 .

Identification of a conserved erythroid specific domain of histone acetylation across the α-globin gene cluster

B M Turner, B. Turner, D. Higgs, 2001, Proceedings of the National Academy of Sciences of the United States of America.

Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease

D. Higgs, J. Sharpe, H. Ayyub, 2003, Nature Genetics.

alpha-thalassemia resulting from a negative chromosomal position effect.

D. Higgs, J. Sharpe, J. Sloane-Stanley, 2000, Blood.

Globin gene activation during haemopoiesis is driven by protein complexes nucleated by GATA‐1 and GATA‐2

G. Blobel, J. Hughes, D. Higgs, 2004, The EMBO journal.

Tissue-specific histone modification and transcription factor binding in alpha globin gene expression.

I. Dunham, Christoph M. Koch, J. Hughes, 2007, Blood.

Analysis of the human alpha globin upstream regulatory element (HS‐40) in transgenic mice.

D. Higgs, J. Sharpe, H. Ayyub, 1992, The EMBO journal.

Analysis of the human alpha-globin gene cluster in transgenic mice.

P. Vyas, D. Higgs, J. Sharpe, 1993, Proceedings of the National Academy of Sciences of the United States of America.

Long‐term haemopoiesis in human fetal liver cell cultures

M. Cappellini, W. Wood, C. Potter, 1984, British Journal of Haematology.

Characterization of β-globin mRNA in the β0 thalassemias

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

Understanding erythroid differentiation

D. Higgs, W. Wood, Douglas R. Higgs, 1993, Current Biology.

Skeletal analysis of the Fgfr3P244R mouse, a genetic model for the Muenke craniosynostosis syndrome

Gillian M Morriss-Kay, Christian Babbs, S. Twigg, 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

Thalassemia Unlinked to the @-Globin Gene in an English Family

Wickramasinghe, W. Wood, M. Galvin, 2003 .

Contrasting effects of alpha and beta globin regulatory elements on chromatin structure may be related to their different chromosomal environments.

P. Vyas, D. Higgs, J. Sharpe, 1995, The EMBO journal.

Fetal hemopoietic-cell transplantation in sheep: an approach to the cellular control of hemoglobin switching.

W. Wood, C. Bunch, S. Kelly, 1985, Progress in clinical and biological research.

Globin gene switching in transgenic mice carrying HS2-globin gene constructs.

N. Roberts, J. Sharpe, J. Sloane-Stanley, 1997, Blood.

An in vitro system for expression analysis of mutations of the β‐globin gene: validation and application to two mutations in the 5′ UTR

J. Sloane-Stanley, S. Thein, W. Wood, 1999, British journal of haematology.

Analysis of an inversion within the human beta globin gene cluster.

R. W. Jones, D. Weatherall, W. Wood, 1985, Nucleic acids research.

Analysis of the human a-globin gene cluster in transgenic mice

D. Higgs, J. Sharpe, W. Wood, 2005 .

Role of upstream DNase I hypersensitive sites in the regulation of human alpha globin gene expression.

P. Vyas, D. Higgs, J. Sharpe, 1993, Blood.

The Mouse a-Globin Locus Regulatory Element

Sharpe, W. Wood, R. D., 2022 .

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.

A. Wilkie, D. Higgs, J. Sharpe, 1990, Blood.

CHAPTER 15 – Congenital dyserythropoietic anemias

W. Wood, G. Hall, R. Renella, 2011 .

Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.

D. Ferguson, L. Bird, D. Higgs, 2010, Blood.

Evidence of genetic heterogeneity in congenital dyserythropoietic anaemia type I

P. Vyas, D. Higgs, W. Wood, 2006, British journal of haematology.

Deletion of the mouse alpha-globin regulatory element (HS -26) has an unexpectedly mild phenotype.

D. Higgs, J. Sharpe, J. Sloane-Stanley, 2002, Blood.

Established epigenetic modifications determine the expression of developmentally regulated globin genes in somatic cell hybrids

N. Roberts, J. Sharpe, J. Sloane-Stanley, 1995, Molecular and cellular biology.

Enhancer deletion generates cellular phenotypic diversity due to bimodal gene expression.

J. Sharpe, J. Sloane-Stanley, M. De Gobbi, 2017, Blood cells, molecules & diseases.

The mouse alpha-globin locus regulatory element.

D. Higgs, J. Sharpe, W. Wood, 1995, Blood.

Regulation of human embryonic globin genes zeta 2 and epsilon in stably transformed mouse erythroleukemia cells.

P. Vyas, D. Higgs, J. Sharpe, 1992, Blood.

Globin gene expression in Hb Lepore‐BAC transgenic mice

D. Weatherall, N. Roberts, J. Sloane-Stanley, 2006, British Journal of Haematology.

Chromosome looping at the human alpha-globin locus is mediated via the major upstream regulatory element (HS -40).

D. Higgs, J. Sharpe, J. Sloane-Stanley, 2009, Blood.

The complexities of β globin gene regulation

W. Wood, 1996 .

How transcriptional and epigenetic programmes are played out on an individual mammalian gene cluster during lineage commitment and differentiation.

J. Hughes, D. Higgs, M. De Gobbi, 2006, Biochemical Society symposium.

a-Thalassemia Caused by a Large ( 62 kb ) Deletion Upstream of the Human a Globin Gene Cluster

Sharpe, V. Buckle, H. Ayyub, 2003 .

A Single 13-Globin LocusControl RegionElement (5'Hypersensitive Site2)IsSufficient forDevelopmental Regulation ofHumanGlobin GenesinTransgenic Mice

J. Sharpe, W. Wood, J. Lida, 1992 .

for allograft rejection in peripheral blood samples Interference of globin genes with biomarker discovery

W. Xiao, Ronald W. Davis, A. Nandi, 2015 .

Instability of beta E-messenger RNA during erythroid cell maturation in hemoglobin E homozygotes.

W. Wood, P. Winichagoon, J. Traeger, 1982, The Journal of clinical investigation.

Nprl3 is required for normal development of the cardiovascular system

Monika S. Kowalczyk, C. Ponting, S. Bhattacharya, 2012, Mammalian Genome.

Mutational analysis of the CDAN1 gene in familial and sporadic congenital dyserythropoietic anaemia type 1

P. Vyas, H. Tamary, W. Wood, 2003 .

Proximal promoter elements of the human zeta-globin gene confer embryonic-specific expression on a linked reporter gene in transgenic mice.

J. Sharpe, L. Pearson, N. Proudfoot, 1996, Nucleic acids research.

Tissue-specific histone modification and transcription factor binding in alpha globin gene expression.

I. Dunham, Christoph M. Koch, J. Hughes, 2007, Blood.

Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis

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

Association between active genes occurs at nuclear speckles and is modulated by chromatin environment

F. Iborra, J. Hughes, D. Higgs, 2008 .

Association between active genes occurs at nuclear speckles and is modulated by chromatin environment

F. Iborra, J. Hughes, D. Higgs, 2008 .

Characterization of the major regulatory element upstream of the human alpha-globin gene cluster

A. Jarman, D. Higgs, J. Sharpe, 1991, Molecular and cellular biology.

A major positive regulatory region located far upstream of the human alpha-globin gene locus.

A. Jarman, D. Higgs, J. Sharpe, 1990, Genes & development.

Fetal Haemoglobin Production and the Sickle Gene in the Oases of Eastern Saudi Arabia

D. Weatherall, W. Wood, M. Pembrey, 1978, British journal of haematology.

The α‐Thalassemias

P. Vyas, A. Wilkie, D. Higgs, 1990, Annals of the New York Academy of Sciences.

The Patterns of Fetal Haemoglobin Production in Leukaemia

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

Transcriptional regulation of GATA1

P. Vyas, W. Wood, C. Porcher, 2007 .

The developmental genetics of human hemoglobin.

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

Unusually severe heterozygous beta-thalassemia: evidence for an interacting gene affecting globin translation.

S. Thein, W. Wood, S. Watt, 1998, Blood.

Global gene expression analysis of human erythroid progenitors.

A. Nandi, S. McGowan, D. Higgs, 2011, Blood.

Coregulated human globin genes are frequently in spatial proximity when active

F. Iborra, D. Higgs, A. Atzberger, 2006, The Journal of cell biology.

Disorders of Hemoglobin: The Molecular Basis of β Thalassemia, δβ Thalassemia, and Hereditary Persistence of Fetal Hemoglobin

S. Thein, W. Wood, 2009 .