Literature DB >> 13373175

X-chromosomal ocular albinism in a Dutch family.

J VAN DEN BOSCH, P J WAARDENBURG.   

Abstract

Entities:  

Keywords:  ALBINISM/heredity

Mesh:

Year:  1956        PMID: 13373175     DOI: 10.1111/j.1469-1809.1971.tb00270.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


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  7 in total

1.  Sex chromatin and gene action in the mammalian X-chromosome.

Authors:  M F LYON
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

2.  Nystagmus in a female carrier of ocular albinism.

Authors:  W G Pearce; G J Johnson; J G Gillan
Journal:  J Med Genet       Date:  1972-03       Impact factor: 6.318

3.  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

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

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

5.  Measurable linkage between ocular albinism and Xg.

Authors:  P J Fialkow; E R Giblett; A G Motulsky
Journal:  Am J Hum Genet       Date:  1967-01       Impact factor: 11.025

6.  Vision in albinism.

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

7.  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

  7 in total

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