Prenatal ultrasound phenotypic and genetic etiology of the 17q12 microduplication syndrome

• Glavni autori: Meiying Cai (Autor), Min Lin (Autor), Nan Guo (Autor), Meimei Fu (Autor), Liangpu Xu (Autor), Na Lin (Autor), Hailong Huang (Autor)
• Format: Knjiga
• Izdano: Frontiers Media S.A., 2022-08-01T00:00:00Z.
• Teme: article
• Online pristup: Connect to this object online.

BackgroundSeveral studies have reported on the clinical phenotype of the 17q12 microduplication syndrome, a rare autosomal dominant genetic disorder, in children and adults, but few have reported on its prenatal diagnosis. This study analyzed the prenatal ultrasound phenotypes of the 17q12 microdupl...