Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay

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Human Genetics, Vol. 130, Iss. 4, 2011-10 ,pp. : 517-528

Springer Publishing Company

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Variable Penetrance of the 15q11.2 BP1-BP2 Microduplication in a Family with Cognitive and Language Impairment

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Molecular Syndromology, Vol. 8, Iss. 3, 2017-04 ,pp. : 139-147

Karger

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A 1-bp deletion in the C-crystallin leads to dominant cataracts in mice

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Mammalian Genome, Vol. 21, Iss. 7-8, 2010-08 ,pp. : 361-369

Springer Publishing Company

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Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population

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Genomic inversions of human chromosome 15q11–q13 in mothers of Angelman syndrome patients with class II (BP2/3) deletions

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