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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

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

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 353 KB
Volume: 146A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32447

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