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Array-CGH detection of a de novo 0.8Mb deletion in 19q13.32 associated with mental retardation, cardiac malformation, cleft lip and palate, hearing loss and multiple dysmorphic features.

Bibliographic reference Leal, Teresinha ; Andrieux, Joris ; Duban-Bedu, Bénédicte ; Bouquillon, Sonia ; Brevière, Georges-Marie ; et. al. Array-CGH detection of a de novo 0.8Mb deletion in 19q13.32 associated with mental retardation, cardiac malformation, cleft lip and palate, hearing loss and multiple dysmorphic features.. In: European journal of medical genetics, Vol. 52, no. 1, p. 62-6 (2009)
Permanent URL http://hdl.handle.net/2078.1/19698