Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction

• Asıl Yazarlar: Chih-Ping Chen (Yazar), Yi-Ning Su (Yazar), Yi-Yung Chen (Yazar), Schu-Rern Chern (Yazar), Yu-Peng Liu (Yazar), Pei-Chen Wu (Yazar), Chen-Chi Lee (Yazar), Yu-Ting Chen (Yazar), Wayseen Wang (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: Elsevier, 2011-09-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Objective: To present prenatal diagnosis of chromosome 1p32-p31 deletion syndrome with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction and to review the literature. Materials, Methods, and Results: A 26-year-old...