Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndrome-Reference-Cited by-同舟云学术

Array-CGH in a series of 30 patients with mental retardation, dysmorphic features, and congenital malformations detected an interstitial 1p22.2-p31.1 deletion in a patient with features overlapping the Goldenhar syndrome

Published:2008-08-15 Issue:16 Volume:146A Page:2109-2115
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Callier P.,Faivre L.,Thauvin-Robinet C.,Marle N.,Mosca A.L.,D'Athis P.,Guy J.,Masurel-Paulet A.,Joly L.,Guiraud S.,Teyssier J.R.,Huet F.,Mugneret F.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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5. Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation;Friedman;Am J Hum Genet,2006

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