B. Jay

发表

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14.

A. Bird, M. Jay, A. Wright, 1987, American journal of human genetics.

Genetic heterogeneity of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in families with familial adenomatous polyposis.

S. Hodgson, D. Bishop, B. Jay, 1994, Journal of medical genetics.

Pigmented lesions of the retinal pigment epithelium and familial adenomatous polyposis

K. Neale, P. Polkinghorne, G. Schoeppner, 1990, Eye.

Partial galactose disorders in families with premature cataracts.

A. Winder, N. Rice, I. Menzies, 1983, Archives of disease in childhood.

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation

A. Bird, M. Jay, A. Wright, 1986, Human Genetics.

Retinitis pigmentosa families showing apparent X linked inheritance but unlinked to the RP2 or RP3 loci.

A. Bird, M. Jay, A. Wright, 1994, Journal of medical genetics.

Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

H. J. Evans, A. Bird, M. Jay, 1991, Journal of medical genetics.

Molecular genetic approaches to the analysis of human ophthalmic disease

D. Cooper, M. Jay, S. Bhattacharya, 1987, Eye.

Nine generations of a family with autosomal dominant retinitis pigmentosa and evidence of variable expressivity from census records.

A. Bird, M. Jay, B. Jay, 1992, Journal of medical genetics.

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

F. Cremers, M. Jay, A. Wright, 1990, American journal of human genetics.

Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients.

T. Rosenberg, F. Cremers, H. Ropers, 1994, Human molecular genetics.

Prenatal diagnosis of X-linked choroideremia with mental retardation, associated with a cytologically detectable X-chromosome deletion

M. Pembrey, J. Goodship, M. Bobrow, 1987, Human Genetics.

Autosomal dominant retinitis pigmentosa: four new mutations in rhodopsin, one of them in the retinal attachment site.

A. Bird, M. Jay, S. Bhattacharya, 1991, Genomics.

No evidence for linkage between late onset autosomal dominant retinitis pigmentosa and chromosome 3 locus D3S47 (C17): evidence for genetic heterogeneity.

H. J. Evans, A. Bird, M. Jay, 1990, Genomics.

In-utero diagnosis of Norrie disease by ultrasonography.

M. Jay, J. Vaughan, B. Jay, 1993, Ophthalmic paediatrics and genetics.

Linkage studies and deletion screening in choroideremia.

H. J. Evans, R. Nussbaum, M. Jay, 1990, Journal of medical genetics.

Relapse following goniotomy for congenital glaucoma due to trabecular dysgenesis

R. Wyse, I. Russell-Eggitt, N. Rice, 1992, Eye.

A genetic linkage study of choroideremia.

M. Jay, A. Wright, M. Dempster, 1986, Ophthalmic paediatrics and genetics.

Macromelanosomes in X‐linked ocular albinism

A. Garner, B. Jay, B. S. JAY, 1980, Histopathology.

Leber's hereditary optic neuropathy

B. Jay, 1990, Eye.

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families.

H. J. Evans, M. Jay, S. Bhattacharya, 1994, American journal of human genetics.

Heterogeneity Analysis in40X-LinkedRetinitis Pigmentosa Families

M. Jay, M. Dempster, A. Carothers, 1994 .