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Q36800533-0DA9C99B-B3F5-4B76-B12B-B0BE084F28C4
Q36800533-0DA9C99B-B3F5-4B76-B12B-B0BE084F28C4
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http://www.wikidata.org/entity/statement/Q36800533-0DA9C99B-B3F5-4B76-B12B-B0BE084F28C4
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs
P2860
Q36800533-0DA9C99B-B3F5-4B76-B12B-B0BE084F28C4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36800533-0DA9C99B-B3F5-4B76-B12B-B0BE084F28C4
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wasDerivedFrom
656b7390a877e33870cca6e210210cb7701be2a9
P2860
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria