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

✍ Scribed by Teresinha Leal; Joris Andrieux; Bénédicte Duban-Bedu; Sonia Bouquillon; Georges-Marie Brevière; Bruno Delobel


Book ID
116433135
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
384 KB
Volume
52
Category
Article
ISSN
1769-7212

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