Congenital Hypotonia in a Child With a De Novo 22q13 Monosomy and 2pter Duplication: A Clinical and Molecular Genetic Study

Published 2010 View Full Article

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Title
Congenital Hypotonia in a Child With a De Novo 22q13 Monosomy and 2pter Duplication: A Clinical and Molecular Genetic Study
Authors
Keywords
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Journal
JOURNAL OF CHILD NEUROLOGY
Volume 26, Issue 2, Pages 235-238
Publisher
SAGE Publications
Online
2010-10-05
DOI
10.1177/0883073810381444
References
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