Literature DB >> 13740435

[On the familial appearance of congenital pseudoglioma].

G REICHEL.   

Abstract

Entities:  

Keywords:  BRAIN/abnormalities; VITREOUS BODY/abnormalities

Mesh：

Year:  1960        PMID： 13740435

Source DB:  PubMed          Journal:  Arch Kinderheilkd        ISSN： 0003-9179


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  2 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.

Authors:  C I Phillips; M Newton; J Duvall; S Holloway; A M Levy
Journal:  Br J Ophthalmol       Date:  1986-04       Impact factor: 4.638
  2 in total

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