## 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
✦ LIBER ✦
Congenital diaphragmatic hernia and a complex heart defect in association with Wolf–Hirschhorn syndrome
✍ Scribed by Juliane Tautz; Danielle Veenma; Bert Eussen; Linda Joosen; Pino Poddighe; Dick Tibboel; Annelies de Klein; Thomas Schaible
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 192 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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