Genotype–phenotype correlations in hereditary familial retinoblastoma-Reference-Cited by-同舟云学术

Genotype–phenotype correlations in hereditary familial retinoblastoma

Published:2007 Issue:3 Volume:28 Page:284-293
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Taylor Melissa,Dehainault Catherine,Desjardins Laurence,Doz François,Levy Christine,Sastre Xavier,Couturier Jérôme,Stoppa-Lyonnet Dominique,Houdayer Claude,Gauthier-Villars Marion

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference56 articles.

1. A possible hot spot in exon 21 of the retinoblastoma gene predisposing to a low penetrant retinoblastoma phenotype?

2. Spectrum of gross deletions and insertions in theRB1 gene in patients with retinoblastoma and association with phenotypic expression

3. Spectrum of germline RB1 gene mutations in Spanish retinoblastoma patients: Phenotypic and molecular epidemiological implications

4. Identification of 26 new constitutionalRB1gene mutations in Spanish, Colombian, and Cuban retinoblastoma patients

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