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

• Main Authors: Chih-Ping Chen (Author), Yi-Ning Su (Author), Yi-Yung Chen (Author), Schu-Rern Chern (Author), Yu-Peng Liu (Author), Pei-Chen Wu (Author), Chen-Chi Lee (Author), Yu-Ting Chen (Author), Wayseen Wang (Author)
• Format: Book
• Published: Elsevier, 2011-09-01T00:00:00Z.
• Subjects: article
• Online Access: 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...