A novel maternally inherited 8q24.3 and a rare paternally inherited 14q23.3 CNVs in a family with neurodevelopmental disorders

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 8, 2015-08 ,pp. : 1921-1926

John Wiley & Sons Inc

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Monozygotic twins with a de novo 0.32 Mb 16q24.3 deletion, including TUBB3 presenting with developmental delay and mild facial dysmorphism but without overt brain malformation

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2731-2736

John Wiley & Sons Inc

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De Novo interstitial deletion 13q33.3q34 in a male patient with double outlet right ventricle, microcephaly, dysmorphic craniofacial findings, and motor and developmental delay

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John Wiley & Sons Inc

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Report on a Patient with a 12q24.31 Microdeletion Inherited from an Insulin-Dependent Diabetes Mellitus Father

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Molecular Syndromology, Vol. 4, Iss. 3, 2013-01 ,pp. : 136-142

Karger

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A 10q21.3q22.2 microdeletion identified in a patient with severe developmental delay and multiple congenital anomalies including congenital heart defects

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CONGENITAL ANOMALIES, Vol. 58, Iss. 1, 2018-01 ,pp. : 36-38

John Wiley & Sons Inc

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