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Three patients with Wolf-Hirschhorn syndrome carrying a satellited chromosome 4p

✍ Scribed by Desheng Liang; Zhongmin Zhou; Dahua Meng; Juan Du; Juan Wen; Norio Niikawa; Lingqian Wu

Book ID
112009318
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
929 KB
Volume
94
Category
Article
ISSN
1542-0752

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## Abstract ## BACKGROUND Wolf‐Hirschhorn syndrome (WHS) is a well‐known genetic condition characterized by typical facial anomalies, midline defects, skeletal anomalies, prenatal and postnatal growth retardation, hypotonia, mental retardation, and seizures. Affected patients with a microdeletion