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A novel 800 kb microduplication of chromosome 16q22.1 resulting in learning disability and epilepsy may explain phenotypic variability in a family with 15q13 microdeletion

✍ Scribed by Siddharth Banka; Gregory J. Fitzgibbon; Lorraine Gaunt; Wendy J. Rankin; Jill Clayton-Smith


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
165 KB
Volume
155
Category
Article
ISSN
1552-4825

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