Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound

• Автори: Chih-Ping Chen (Автор), Shu-Yuan Chang (Автор), Chen-Ju Lin (Автор), Schu-Rern Chern (Автор), Peih-Shan Wu (Автор), Shin-Wen Chen (Автор), Shih-Ting Lai (Автор), Tzu-Yun Chuang (Автор), Wen-Lin Chen (Автор), Chien-Wen Yang (Автор), Wayseen Wang (Автор)
• Формат: Книга
• Опубліковано: Elsevier, 2018-10-01T00:00:00Z.
• Предмети: article
• Онлайн доступ: Connect to this object online.

Objective: We present prenatal diagnosis of a familial 5p14.3-p14.1 deletion in a fetus with congenital heart disease on prenatal ultrasound. Case report: A 33-year-old woman underwent amniocentesis at 18 weeks of gestation because of fetal ventricular septal defect (VSD) and echogenic bowel on pren...