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

By Burnside Rachel   Pasion Romela   Mikhail Fady   Carroll Andrew   Robin Nathaniel   Youngs Erin   Gadi Inder   Keitges Elizabeth   Jaswaney Vikram   Papenhausen Peter   Potluri Venkateswara   Risheg Hiba   Rush Brooke   Smith Janice   Schwartz Stuart   Tepperberg James   Butler Merlin  

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

Springer Publishing Company

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Deletion of 15q11.2(BP1‐BP2) region: Further evidence for lack of phenotypic specificity in a pediatric population

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2098-2102

John Wiley & Sons Inc

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Cognitive Deficit, Learning Difficulties, Severe Behavioral Abnormalities and Healed Cleft Lip in a Patient with a 1.2-Mb Distal Microduplication at 22q11.2

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Molecular Syndromology, Vol. 4, Iss. 6, 2013-08 ,pp. : 292-296

Karger

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Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family

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Karger

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

By Estivill X.  

Human Molecular Genetics, Vol. 12, Iss. 8, 2003-04 ,pp. : 849-858

Oxford University Press

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