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A novel 1p31.3p32.2 deletion involving theNFIAgene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum

✍ Scribed by Udo Koehler; Elke Holinski-Feder; Birgit Ertl-Wagner; Juergen Kunz; Arpad von Moers; Hubertus von Voss; Chayim Schell-Apacik

Book ID: 106121891
Publisher: Springer
Year: 2009
Tongue: English
Weight: 270 KB
Volume: 169
Category: Article
ISSN: 0340-6997
DOI: 10.1007/s00431-009-1057-2

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