Literature DB >> 752489

Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies.

P M Conneally, A F Wilson, A D Merritt, E M Helveston, C G Palmer, L Y Wang.   

Abstract

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Year:  1978        PMID： 752489     DOI： 10.1159/000130957

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  6 in total

1.  The genetics of cataract: our vision becomes clearer.

Authors:  J F Hejtmancik
Journal:  Am J Hum Genet       Date:  1998-03       Impact factor: 11.025

2.  A locus for a human hereditary cataract is closely linked to the gamma-crystallin gene family.

Authors:  N H Lubsen; J H Renwick; L C Tsui; M L Breitman; J G Schoenmakers
Journal:  Proc Natl Acad Sci U S A       Date:  1987-01       Impact factor: 11.205

3.  Autosomal dominant zonular cataract with sutural opacities localized to chromosome 17q11-12.

Authors:  T Padma; R Ayyagari; J S Murty; S Basti; T Fletcher; G N Rao; M Kaiser-Kupfer; J F Hejtmancik
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

4.  Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36.

Authors:  H Eiberg; A M Lund; M Warburg; T Rosenberg
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

5.  Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I.

Authors:  L R Griffiths; M B Zwi; J G McLeod; G A Nicholson
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

6.  Novel human CRYGD rare variant in a Brazilian family with congenital cataract.

Authors:  Eugênio Santana de Figueirêdo; Gabriel Gorgone Giordano; Anderson Tavares; Márcio José da Silva; José Paulo Cabral de Vasconcellos; Carlos Eduardo Leite Arieta; Mônica Barbosa de Melo
Journal:  Mol Vis       Date:  2011-08-16       Impact factor: 2.367
  6 in total

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