A. Read

M. Tassabehji, A. Read, C. Paterson, 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Hearing loss and pigmentary disturbances in Waardenburg syndrome with reference to WS Type II

A. Read, V. Newton, X. Liu, 1995, The Journal of Laryngology & Otology.

CLINIC EXPERIENCE OF PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS BY USE OF LINKED DNA PROBES

A. Read, M. Schwarz, A. Ivinson, 1987, The Lancet.

The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.

R. Williamson, A. Read, M. Dixon, 1991, American journal of human genetics.

What can be offered to couples at (possibly) increased genetic risk?

A. Read, D. Donnai, 2012, Journal of Community Genetics.

SOX10 mutations in patients with Waardenburg-Hirschsprung disease

Giovanni Romeo, Gert Matthijs, Eric Legius, 1998, Nature Genetics.

Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene

Andrew P. Read, M. Tassabehji, A. Read, 1994, Nature Genetics.

A gene for Waardenburg Syndrome type 2 maps close to the human homologue of the microphthalmia gene at chromosome 3p12–p14.1

X. Liu, A. Read, A. Hughes, 1994, Nature Genetics.

Recurrent neural tube defects, risk factors and vitamins.

A. Read, M. Seller, R. Harris, 1986, Archives of disease in childhood.

POSSIBLE MATERNAL EFFECT IN GENETIC SUSCEPTIBILITY TO MYASTHENIA GRAVIS

A. Read, R. Metcalfe, P. Dyer, 1986, The Lancet.

Is there a genetic basis for Fuchs' heterochromic uveitis? Discordance in monozygotic twins.

A. Read, N. Jones, N. P. Jones, 1992, The British journal of ophthalmology.

Elastin: mutational spectrum in supravalvular aortic stenosis

C. Cytrynbaum, W. Reardon, M. Tassabehji, 2000, European Journal of Human Genetics.

Hypomelanosis of Ito

A. Read, D. Donnai, 1992, The Lancet.

Syndrome of the month Waardenburg syndrome

A. Read, V. Newton, 2004 .

Waardenburg syndrome.

A. Read, V. Newton, V. Newton, 1997, Journal of medical genetics.

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene

R. Balling, M. Tassabehji, T. Strachan, 1992, Nature.

Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

A. Read, C. Mckeown, D. Donnai, 1988, Journal of medical genetics.

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

M. Tassabehji, M. Patton, T. Strachan, 1993, Nature Genetics.

SLUG (SNAI2) deletions in patients with Waardenburg disease.

A. Read, A. Sagrera, M. Sánchez-Martín, 2002, Human molecular genetics.

Waardenburg syndrome type II: phenotypic findings and diagnostic criteria.

A. Read, V. Newton, X. Liu, 1995, American journal of medical genetics.

Localization of a Gene for Waardenburg Syndrome Type I a

A. Read, V. Newton, Rodney Harris, 1991, Annals of the New York Academy of Sciences.

FALSE POSITIVE RESULTS WITH THE QUALITATIVE AMNIOTIC FLUID ACETYLCHOLINESTERASE TEST

A. Read, D. Donnai, S. Fennell, 1981, The Lancet.

Amniotic fluid acetylcholinesterase: a retrospective and prospective study of the qualitative method

A. Read, D. Donnai, R. Harris, 1982, British journal of obstetrics and gynaecology.

Haemangioma of the cord: further cause of raised maternal serum and liquor alpha-fetoprotein.

A. Read, D. Donnai, P. Donnai, 1980, British medical journal.

The presence of multiple regions of homozygous deletion at the CSMD1 locus in oral squamous cell carcinoma question the role of CSMD1 in head and neck carcinogenesis

A. Read, S. Gollin, M. Dixon, 2003, Genes, chromosomes & cancer.

VITAMINS AND NEURAL TUBE DEFECTS

A. Read, M. Seller, G. Oakley, 1983, The Lancet.

932. Nucleotides. Part XLIX. The reduction of the adduct of periodate-oxidised adenosine-5′ phosphate and methylamine

A. Read, D. Brown, 1965 .

New DNA markers in the Huntington's disease gene candidate region

M. MacDonald, H. Lehrach, J. Gusella, 1991, Somatic cell and molecular genetics.

Testing for cystic fibrosis using allelic association.

A. Read, M. Schwarz, A. Ivinson, 1989, Journal of medical genetics.

Molecular genetics in the National Health Service in Britain.

D. Craufurd, T. Strachan, A. Read, 1989, Journal of medical genetics.

Molecular genetics intheNational HealthService inBritain

D. Craufurd, T. Strachan, A. Read, 1989 .

Our place in the tree of life

T. Strachan, A. Read, 1999 .

LIM–kinase deleted in Williams syndrome

M. Tassabehji, A. Read, D. Sheer, 1996, Nature Genetics.

Diagnosis of adult polycystic kidney disease by genetic markers and ultrasonographic imaging in a voluntary family register.

A. Read, R. Elles, R. Harris, 1994, Journal of medical genetics.

True telomeric translocation in a baby with the Prader-Willi phenotype.

A. Reeve, A. Read, P. Sinclair, 1993, American journal of medical genetics.

Molecular biology and the ENT surgeon in the millennium

A. Read, 1998, The Journal of Laryngology & Otology.

Inherited eye disease: cause and late effect.

A. Read, G. Black, D. Trump, 2005, Trends in molecular medicine.

Mutation of the MITF gene in albinism‐deafness syndrome (Tietz syndrome)

M. Tassabehji, R. Winter, A. Read, 1998, Clinical dysmorphology.

Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis

K. Davies, F. Glorieux, A. Read, 1986, Human Genetics.

Linkage analysis of two cloned DNA sequences, DXS197 and DXS207, in hypophosphatemic rickets families.

K. Davies, A. Read, R. Thakker, 1990, Genomics.

Bridging markers defining the map position of X linked hypophosphataemic rickets.

R. Weksberg, K. Davies, F. Glorieux, 1987, Journal of medical genetics.

112 Waardenburg Syndrome

A. Read, 1998 .

Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q.

L. Farrer, C. Baldwin, A. Read, 1995, Journal of medical genetics.

Chromosome 13 q deletion with Waardenburg syndrome : further evidence for a gene involved in neural crest function on 13 q

L. Farrer, C. Baldwin, A. Read, 2022 .

Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome

A. Karmiloff-Smith, M. Tassabehji, A. Read, 2003, Journal of medical genetics.

TO JMG Using case study comparisons to explore genotype-phenotype correlations in Williams-Beuren syndrome

A. Karmiloff-Smith, M. Tassabehji, A. Read, 2003 .

Williams syndrome: use of chromosomal microdeletions as a tool to dissect cognitive and physical phenotypes.

A. Karmiloff-Smith, J. Grant, W. Reardon, 1999, American journal of human genetics.

Norrie disease resulting from a gene deletion: clinical features and DNA studies.

A. Read, R. Mountford, D. Donnai, 1988, Journal of medical genetics.

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities

A. Janssens, A. Cambon-Thomsen, M. Krawczak, 2011, European Journal of Human Genetics.

DLC1 is unlikely to be a primary target for deletions on chromosome arm 8p22 in head and neck squamous cell carcinoma.

A. Read, S. Gollin, N. Thakker, 2004, Cancer letters.

PAX genes in human developmental anomalies

A. Read, V. Heyningen, 1994 .

EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY

K. Davies, A. Read, P. Harper, 1987, The Lancet.

National Coordination of Molecular Genetic Services

A. Read, 1991 .

Genetic mapping of complex characters

T. Strachan, A. Read, 1999 .

Principles of DNA-based prenatal diagnosis of cystic fibrosis: an introduction for the clinician.

A. Read, 1987, Journal of the Royal Society of Medicine.

GTF2IRD1 in Craniofacial Development of Humans and Mice

Peter Hammond, Dian Donnai, Annette Karmiloff-Smith, 2005, Science.

A transcription factor involved in skeletal muscle gene expression is deleted in patients with Williams syndrome

M. Tassabehji, C. Wilmot, A. Read, 1999, European Journal of Human Genetics.

Identification of mutations in CUL7 in 3-M syndrome

A. Munnich, P. Scambler, R. Hennekam, 2005, Nature Genetics.

Beckwith-Wiedemann syndrome.

L. Gaunt, A. Read, A. Slavotinek, 1992, Journal of medical genetics.

Neural‐tube defects and vitamins: the need for a randomized clinical trial

A. Read, M. Seller, R. Harris, 1985, British journal of obstetrics and gynaecology.

Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomas

D. Evans, A. Read, R. Ramsden, 2002, Journal of medical genetics.

Brachydactyly and mental retardation: an Albright hereditary osteodystrophy-like syndrome localized to 2q37.

J. Flint, A. Read, R. Trembath, 1995, American journal of human genetics.

Differential diagnosis of type 2 neurofibromatosis: molecular discrimination of NF2 and sporadic vestibular schwannomas.

D. Evans, A. Read, R. Ramsden, 1998, Journal of medical genetics.

New uncertainties in prenatal screening for neural tube defect.

A. Read, R. Harris, 1981, British medical journal.

Linkage analysis in 16 families with incontinentia pigmenti.

E. Hatchwell, S. Kenwrick, A. Read, 1997 .

Seventh International Congress of Human Genetics. Update on the X chromosome

A. Read, 1987 .

A register based system for gene tracking in Duchenne muscular dystrophy.

A. Read, R. Mountford, R. Elles, 1986, Journal of medical genetics.

Preimplantation diagnosis with the polymerase chain reaction.

A. Read, D. Donnai, 1989, BMJ.

Matching for properdin factor B (Bf) in renal transplantation.

A. Read, N. Mallick, P. Dyer, 1981, Transplantation.

Pax genes — Paired feet in three camps

A. Read, 1995, Nature Genetics.

The role of cathepsin C in Papillon‐Lefèvre syndrome, prepubertal periodontitis, and aggressive periodontitis

Andrew P Read, Philip Sloan, Richard Widmer, 2004, Human mutation.

The genetics of otosclerosis: pedigree studies and linkage analysis.

A. Read, R. Ramsden, S. Saeed, 2007, Advances in oto-rhino-laryngology.

Gene linkage and genetic deafness.

K. Steel, C. Cremers, H. Brunner, 1995, International journal of pediatric otorhinolaryngology.

Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)

M. McCarthy, C. Larsson, B. Teh, 1997, Human Genetics.

Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.

K. Davies, A. Read, T. Flint, 1988, Journal of medical genetics.

Patterns of exon deletions in Duchenne and Becker muscular dystrophy

K. Davies, S. Kenwrick, A. Read, 1988, Human Genetics.

Structure and expression of the Huntington's disease gene: Evidence against simple inactivation due to an expanded CAG repeat

R. Durbin, D. Church, M. MacDonald, 1994, Somatic cell and molecular genetics.

Basic principles of nucleic acid structure and gene expression

T. Strachan, A. Read, 2018, Human Molecular Genetics.

VITAMIN SUPPLEMENTATION AND NEURAL TUBE DEFECTS

A. Read, E. Knox, M. Seller, 1983, The Lancet.

Neural tube defect recurrence after 'partial' vitamin supplementation.

A. Read, M. Seller, R. Harris, 1989, Journal of medical genetics.

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations

K. Arnos, A. Pandya, L. Farrer, 1998, Human Genetics.

Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1–22.2)

H. Lehrach, K. Davies, A. Read, 1994, Human Genetics.

New markers for linkage analysis of X-linked hypophosphataemic rickets

S. Meier-Ewert, H. Lehrach, K. Davies, 1993, Human Genetics.

X-linked and FSH dystrophies in one family

A. Read, B. Lecky, D. Wilcox, 1991, Neuromuscular Disorders.

Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).

T. Meitinger, T. Strom, H. Lehrach, 1997, Human molecular genetics.

Reply to “Mutations of PAX3 unlikely in Waardenburg syndrome type 2”

M. Patton, A. Read, V. Newton, 1993, Nature Genetics.

Thalidomide may be a mutagen

A. Read, W. Mcbride, 1994, BMJ.

Mapping of the X linked form of hyper IgM syndrome (HIGM1)

R. Levinsky, A. Read, S. Malcolm, 1993, Journal of medical genetics.

VITAMIN SUPPLEMENTS AND NEURAL TUBE DEFECTS

A. Read, M. Seller, R. Smithells, 1982, The Lancet.

COMPARISON OF PREGNANCY OUTCOME AFTER AMNIOCENTESIS FOR PREVIOUS NEURAL TUBE DEFECT OR RAISED MATERNAL SERUM ALPHAFETOPROTEIN

A. Read, D. Donnai, R. Harris, 1980, British journal of obstetrics and gynaecology.

Three DNA markers for hypophosphataemic rickets

K. Davies, G. Camerino, A. Read, 1992, Human Genetics.

The gene for X-linked hypophosphataemic rickets maps to a 200–300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE)

J. Weissenbach, H. Lehrach, K. Davies, 1996, Human Genetics.

Analysis of Human Genetic Linkage

A. Read, 1992 .

How clinicians add to knowledge of development

A. Read, D. Donnai, 2003, The Lancet.

X linked or autosomal recessive? A new approach to an old problem.

A. Read, 1989, Journal of medical genetics.

Apparent prevention of neural tube defects by periconceptional vitamin supplementation.

A. Read, M. Seller, R. Harris, 1981, Archives of disease in childhood.

PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse.

M. Tassabehji, T. Strachan, A. Read, 1994, Human molecular genetics.

Guidelines for DNA banking. Report of the Clinical Genetics Society working party on DNA banking.

A. Read, S. Malcolm, J. Yates, 1989, Journal of medical genetics.

Theory of Population Genetics and Evolutionary Ecology: An Introduction

A. Read, 1981 .

Stress after amniocentesis for high serum alpha-fetoprotein concentrations.

A. Read, D. Donnai, R. Harris, 1980, British medical journal.

Recombination or heterogeneity: is there a second locus for adult polycystic kidney disease?

A. Read, R. Elles, R. Harris, 1990, Journal of medical genetics.

polycystic kidney disease ? second locus for adult heterogeneity : is there a Recombination or and

A. Read, R. Elles, R. Harris, 2022 .

Hereditary deafness: lessons for developmental studies and genetic diagnosis

A. Read, 2000, European Journal of Pediatrics.

What can be offered to couples at (possibly) increased genetic risk?

A. Read, D. Donnai, 2012, Journal of Community Genetics.

Huntington's disease: testing the test

A. Read, 1993, Nature Genetics.

Olympic freak show?

A. Read, 1997 .