Interaction between a chromosome 10RETenhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association-Reference-Cited by-同舟云学术

Interaction between a chromosome 10RETenhancer and chromosome 21 in the Down syndrome-Hirschsprung disease association

Published:2009-03-20 Issue:5 Volume:30 Page:771-775
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Arnold Stacey,Pelet Anna,Amiel Jeanne,Borrego Salud,Hofstra Robert,Tam Paul,Ceccherini Isabella,Lyonnet Stanislas,Sherman Stephanie,Chakravarti Aravinda

Funder

“Holes for Hirschsprung” Fundraiser

Fondation Jérôme Lejeune

Agence Nationale de la Recherche (HirGenet)

U.S. National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference15 articles.

1. NFAT dysregulation by increased dosage of DSCR1 and DYRK1A on chromosome 21;Arron;Nature,2006

2. Methods for studying recombination on chromosomes that undergo nondisjunction;Chakravarti;Genomics,1987

3. Molecular mapping of twenty-four features of Down syndrome on chromosome 21;Delabar;Eur J Hum Genet,1993

4. Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease;de Pontual;Hum Mut,2007

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