Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result

• المؤلفون الرئيسيون: Chih-Ping Chen (مؤلف), Tsang-Ming Ko (مؤلف), Liang-Kai Wang (مؤلف), Schu-Rern Chern (مؤلف), Peih-Shan Wu (مؤلف), Shin-Wen Chen (مؤلف), Fang-Tzu Wu (مؤلف), Li-Feng Chen (مؤلف), Wayseen Wang (مؤلف)
• التنسيق: كتاب
• منشور في: Elsevier, 2021-07-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Objective: We present partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency (NT) and an abnormal maternal serum screening result. Case Re...