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Paper Details

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
N Engl J Med
549
2008
1, 1q21, autism, autism spectrum disorder, cardiac abnormalities, cataracts, children, chromosome 1q21, congenital anomalies, human, human genome, mental retardation, microcephaly, patients, persons, syndromic

Datasets

Release 1.2