The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature-Reference-Cited by-同舟云学术

The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature

Published:2014-11-17 Issue:1 Volume:167 Page:185-189
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jean-Marçais Nolwenn¹²,Decamp Matthieu¹³,Gérard Marion¹,Ribault Virginie²,Andrieux Joris⁴,Kottler Marie-Laure¹³,Plessis Ghislaine¹

Affiliation:

1. Service de Génétique; Hôpital Universitaire de la Côte de Nacre; Caen France

2. Service de Pédiatrie; Hôpital Universitaire de la Côte de Nacre; Caen France

3. UFR de Médecine de Caen; Université de Caen; Caen France

4. Laboratoire de Génétique Médicale; Hôpital Universitaire Jeanne de Flandre; Lille France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36428/fullpdf

Reference11 articles.

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4. Molecular cytogenetic analysis of five 2q37 deletions: Refining the brachydactyly candidate region;Chaabouni;Eur J Med Genet,2006

5. Chromosome 2q37 deletion: clinical and molecular aspects;Falk;Am J Med Genet C Semin Med Genet,2007

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