X-linked ocular albinism-Reference-Cited by-同舟云学术

X-linked ocular albinism

Published:1981-02 Issue:3 Volume:56 Page:299-304
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Jaeger Charlotte,Jay Barrie

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00274683.pdf

Reference14 articles.

1. Falls HF (1951) Sex-linked ocular albinism displaying typical fundus changes in the female heterozygote. Am J Ophthalmol 34:41–50

2. Forsius H, Eriksson AW (1964) Ein neues Augensyndrom mit X-chromosomaler Transmission. Eine Sippe mit Fundus-albinismus, Foveahypoplasie, Nystagmus, Myopie, Astigmatismus und Dyschromatopsie. Klin Monatsbl Augenheilkd 144:447–454

3. Garner A, Jay BS (1980) Macromelanosomes in X-linked ocular albinism. Histopathology 4:243–254

4. Gillespie FD, Covelli B (1963) Carriers of ocular albinism with and without ocular changes. Arch Ophthalmol 70:209–213

5. Jay B, Carruthers J, Treplin MCW, Winder AF (1976) Human albinism. Birth Defects 12 (3):415–426

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1. Abnormalities of Pigmentation;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

2. New insights into ocular albinism type 1 (OA1): Mutations and polymorphisms of the OA1 gene;Human Mutation;2002-01-07

3. Extracutaneous analogies of Blaschko lines;American Journal of Medical Genetics;1999-08-06

4. X-linked ocular albinism: prevalence and mutations – a national study;European Journal of Human Genetics;1998-11

5. OA1 Mutations and Deletions in X-Linked Ocular Albinism;The American Journal of Human Genetics;1998-04