Literature DB >> 14060100

CARRIERS OF OCULAR ALBINISM WITH AND WITHOUT OCULAR CHANGES.

F D GILLESPIE, B COVELLI.   

Abstract

Keywords:  ALBINISM; FUNDUS OCULI; GENETICS, HUMAN; IRIS; OPHTHALMOLOGY; PIGMENTATION; TRANSILLUMINATION

Mesh：

Year:  1963        PMID： 14060100     DOI： 10.1001/archopht.1963.00960050211012

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  6 in total

1.  Genetic mapping of X linked ocular albinism: linkage analysis in British families.

Authors:  S J Charles; A T Moore; J R Yates
Journal:  J Med Genet       Date:  1992-08       Impact factor: 6.318

2.  Clinical features of affected males with X linked ocular albinism.

Authors:  S J Charles; J S Green; J W Grant; J R Yates; A T Moore
Journal:  Br J Ophthalmol       Date:  1993-04       Impact factor: 4.638

3.  X-chromosomal-linked diseases affecting the eye: status of the heterozygote female.

Authors:  A E Krill
Journal:  Trans Am Ophthalmol Soc       Date:  1969

4.  Vision in albinism.

Authors:  C G Summers
Journal:  Trans Am Ophthalmol Soc       Date:  1996

5.  Albinism in childhood: a flash VEP and ERG study.

Authors:  I Russell-Eggitt; A Kriss; D S Taylor
Journal:  Br J Ophthalmol       Date:  1990-03       Impact factor: 4.638

6.  X-linked ocular albinism: a family containing a manifesting heterozygote, and an affected male married to a female with autosomal recessive ocular albinism.

Authors:  C Jaeger; B Jay
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132
  6 in total

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