Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes-Reference-Cited by-同舟云学术

Early-onset obesity and paternal 2pter deletion encompassing the ACP1, TMEM18, and MYT1L genes

Published:2013-10-16 Issue:4 Volume:22 Page:471-479
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Doco-Fenzy Martine,Leroy Camille,Schneider Anouck,Petit Florence,Delrue Marie-Ange,Andrieux Joris,Perrin-Sabourin Laurence,Landais Emilie,Aboura Azzedine,Puechberty Jacques,Girard Manon,Tournaire Magali,Sanchez Elodie,Rooryck Caroline,Ameil Agnès,Goossens Michel,Jonveaux Philippe,Lefort Geneviève,Taine Laurence,Cailley Dorothée,Gaillard Dominique,Leheup Bruno,Sarda Pierre,Geneviève David

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/ejhg2013189.pdf

Reference24 articles.

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3. Ravnan JB, Tepperberg JH, Papenhausen P et al: Subtelomere FISH analysis of 11 688 cases: an evaluation of the frequency and pattern of subtelomere rearrangements in individuals with developmental disabilities. J Med Genet 2006; 43: 478–489.

4. Zou YS, Van Dyke DL, Ellison JW : Microarray comparative genomic hybridization and FISH studies of an unbalanced cryptic telomeric 2p deletion/16q duplication in a patient with mental retardation and behavioral problems. Am J Med Genet A 2007; 143: 746–751.

5. Wu Y, Ji T, Wang J et al: Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation. BMC Med Genet 2010; 11: 72.

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