D. Hewett

发表

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.

R I Richards, S. Schuffenhauer, R. Richards, 1998, Molecular cell.

A new missense mutation of fibrillin in a patient with Marfan syndrome.

B. Sykes, A. Child, D. Hewett, 1994, Journal of Medical Genetics.

Abstracts for the committee on the genetic constitution of chromosome 1

Brien, J. Beckmann, K. Kidd, 1991 .

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 24 of 27)

J. Beckmann, K. Kidd, K. Klinger, 1991 .

Genetic linkage of the Marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5. The International Marfan Syndrome Collaborative Study.

D. Viljoen, R. Devereux, B. Sykes, 1992, The New England journal of medicine.

Abstracts for the committee on the genetic constitution of the X chromosome (Part 3 of 3)

Brien, J. Beckmann, K. Kidd, 1991 .

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

P. R. Boyd, A. Roses, J. Riley, 2001, Genomics.

Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.

R I Richards, M. Leppert, R. Richards, 1997, American journal of human genetics.

Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat

D. Paslier, N. Doggett, R. Richards, 1997, Cell.

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms

Jörg Schmidtke, Kenneth K. Kidd, Jacques S. Beckmann, 1991 .

The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis

N. E. Morton, N. Morton, W. Tapper, 2002, Proceedings of the National Academy of Sciences of the United States of America.

A novel fibrillin mutation in the Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module.

B. Sykes, D. Hewett, J. Lynch, 1993, Human molecular genetics.

Differential allelic expression of a fibrillin gene (FBN1) in patients with Marfan syndrome.

H. Firth, B. Sykes, A. Child, 1994, American journal of human genetics.

Identification of a psoriasis susceptibility candidate gene by linkage disequilibrium mapping with a localized single nucleotide polymorphism map.

A. Roses, J. Riley, C. G. See, 2002, Genomics.

Abstracts for the committee on the genetic constitution of chromosome 6

Brien, J. Beckmann, K. Kidd, 1991 .

Abstracts for the committee on comparative gene mapping

Brien, J. Beckmann, K. Kidd, 1991 .

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 23 of 27)

J. Beckmann, K. Kidd, K. Klinger, 1991 .

Abstracts for the committee on the genetic constitution of chromosome 15

Brien, J. Beckmann, K. Kidd, 1991 .

Report of the DNA committee and catalogues of cloned and mapped genes, markers formatted for PCR and DNA polymorphisms (Part 27 of 27)

J. Beckmann, K. Kidd, K. Klinger, 1991 .