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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities

Ankita Patel and colleagues report microdeletions and microduplications on chromosome 1q21.1 in a series of individuals with features of microcephaly and macrocephaly, as well as developmental delay and neuropsychiatric abnormalities.

Nicola Brunetti-Pierri
Jonathan S Berg
Ankita Patel
Research23 Nov 2008
Nature Genetics

Volume: 40, P: 1466-1471

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