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Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia

Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilms tumor risk, were studied by fluorescence in situ hybridization (FISH), through use of a panel of cosmids encompassing the aniridia-associated PAX6 gene, the Wilms tumor predisposition gene WT1, and...

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Detalhes bibliográficos
Main Authors: Crolla, John A., van Heyningen, Veronica
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2002
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC385089/
https://ncbi.nlm.nih.gov/pubmed/12386836
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