Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Microcephaly and NDE1[original query] |
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Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. PloS one 2013 8 (4): e61365. Tropeano Maria, Ahn Joo Wook, Dobson Richard J B, Breen Gerome, Rucker James, Dixit Abhishek, Pal Deb K, McGuffin Peter, Farmer Anne, White Peter S, Andrieux Joris, Vassos Evangelos, Ogilvie Caroline Mackie, Curran Sarah, Collier David |
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria. PLoS genetics 2013 9 (10): e1003823. Sajan Samin A, Fernandez Liliana, Nieh Sahar Esmaeeli, Rider Eric, Bukshpun Polina, Wakahiro Mari, Christian Susan L, Rivière Jean-Baptiste, Sullivan Christopher T, Sudi Jyotsna, Herriges Michael J, Paciorkowski Alexander R, Barkovich A James, Glessner Joseph T, Millen Kathleen J, Hakonarson Hakon, Dobyns William B, Sherr Elliott |
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- Page last updated:Apr 16, 2024
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