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A homozygous deletion of 8q24.3 including the NIBP gene associated with severe developmental delay, dysgenesis of the corpus callosum, and dysmorphic facial features

✍ Scribed by Arie Koifman; Annette Feigenbaum; Weimin Bi; Lisa G. Shaffer; Jill Rosenfeld; Susan Blaser; David Chitayat


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
213 KB
Volume
152A
Category
Article
ISSN
1552-4825

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