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A newly recognised microdeletion syndrome of 2p15-16.1 manifesting moderate developmental delay, autistic behaviour, short stature, microcephaly, and dysmorphic features: a new patient with 3.2 Mb deletion

JOURNAL OF MEDICAL GENETICS (2009)

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Journal

JOURNAL OF MEDICAL GENETICS
Volume 46, Issue 9, Pages 645-647

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/jmg.2008.059220

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Genetics & Heredity

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