Literature DB >> 191773

Aniridia-Wilms' tumour syndrome.

J François, D Coucke, R Coppieters.   

Abstract

The association of aniridia and Wilms' tumour constitutes a real syndrome, which is genetic. It may either be autosomal dominant or depend on a chromosomal deletion or also, according to Knudson's theory, be due to two mutational events, the initiating mutation being germinal and the promoting mutation being post-zygotical.

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Year:  1977        PMID: 191773     DOI: 10.1159/000308573

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN: 0030-3755            Impact factor:   3.250


  3 in total

Review 1.  Wilms' and associated renal tumors of childhood.

Authors:  K S White; H Grossman
Journal:  Pediatr Radiol       Date:  1991

Review 2.  Microcytogenetics 1984.

Authors:  J de Grouchy; C Turleau
Journal:  Experientia       Date:  1986-10-15

3.  Del11p13/nephroblastoma without aniridia.

Authors:  C Turleau; J de Grouchy; C Nihoul-Fékété; J L Dufier; F Chavin-Colin; C Junien
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

  3 in total

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