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

• প্রধান লেখক: Chih-Ping Chen (লেখক), Yi-Ning Su (লেখক), Yi-Yung Chen (লেখক), Schu-Rern Chern (লেখক), Yu-Peng Liu (লেখক), Pei-Chen Wu (লেখক), Chen-Chi Lee (লেখক), Yu-Ting Chen (লেখক), Wayseen Wang (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Elsevier, 2011-09-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: 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...