Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly

• Ngā kaituhi matua: Pi-Lin Sung (Author), Chia-Ming Chang (Author), Chih-Yao Chen (Author), Peng-Hui Wang (Author), Kuan-Chong Chao (Author), Kuo-Chang Wen (Author), Yung-Yung Cheng (Author), Yueh-Chun Li (Author), Chyi-Chyang Lin (Author)
• Hōputu: Pukapuka
• I whakaputaina: Elsevier, 2012-06-01T00:00:00Z.
• Ngā marau: article
• Urunga tuihono: Connect to this object online.

Objective: To present a prenatal diagnosis of microdeletion 16p13.11 with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly. Case Report: A 41-year-old well-being Taiwanese, nulligravida woman r...