Literature DB >> 5171678

Genetic counselling in sporadic cases of congenital cataract.

S Jensen, E Goldschmidt.   

Abstract

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Mesh：

Year:  1971        PMID： 5171678     DOI： 10.1111/j.1755-3768.1971.tb02963.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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  4 in total

1.  [Genetic counseling in eye diseases (author's transl)].

Authors:  B Burow; U Theile
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1973-11-06

2.  An increase in apoptosis and reduction in αB-crystallin expression levels in the lens underlie the cataractogenesis of Morioka cataract (MCT) mice.

Authors:  Tomohiro Kondo; Naoko Ishiga-Hashimoto; Hiroaki Nagai; Ai Takeshita; Masaki Mino; Hiroshi Morioka; Ken Takeshi Kusakabe; Toshiya Okada
Journal:  Med Mol Morphol       Date:  2011-12-17       Impact factor: 2.309

3.  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

4.  The cell adhesion gene PVRL3 is associated with congenital ocular defects.

Authors:  Salil A Lachke; Anne W Higgins; Maiko Inagaki; Irfan Saadi; Qiongchao Xi; Michelle Long; Bradley J Quade; Michael E Talkowski; James F Gusella; Atsuko Fujimoto; Michael L Robinson; Ying Yang; Quynh T Duong; Irit Shapira; Benny Motro; Jun Miyoshi; Yoshimi Takai; Cynthia C Morton; Richard L Maas
Journal:  Hum Genet       Date:  2011-07-17       Impact factor: 4.132
  4 in total

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