Pre- and postnatal phenotype of 6p25 deletions involving theFOXC1gene-Reference-Cited by-同舟云学术

Pre- and postnatal phenotype of 6p25 deletions involving theFOXC1gene

Published:2012-08-17 Issue:10 Volume:158A Page:2430-2438
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Delahaye Andrée,Khung-Savatovsky Suonavy,Aboura Azzedine,Guimiot Fabien,Drunat Séverine,Alessandri Jean-Luc,Gérard Marion,Bitoun Pierre,Boumendil Julien,Robin Stéphanie,Huel Chan,Guilherme Romain,Serero Stéphane,Gressens Pierre,Elion Jacques,Verloes Alain,Benzacken Brigitte,Delezoide Anne-Lise,Pipiras Eva

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference39 articles.

1. FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation;Aldinger;Nat Genet,2009

2. A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia;Bedoyan;Am J Med Genet Part A,2011

3. Schizophrenia in an adult with 6p25 deletion syndrome;Caluseriu;Am J Med Genet Part A,2006

4. A novel mechanistic spectrum underlies glaucoma-associated chromosome 6p25 copy number variation;Chanda;Hum Mol Genet,2008

5. Mild developmental delay in terminal chromosome 6p deletion;Chen;Am J Med Genet Part A,2004

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