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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
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. MugneretVolume:
146A
Year:
2008
Language:
english
Pages:
7
DOI:
10.1002/ajmg.a.32447
File:
PDF, 353 KB
english, 2008