Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound

• Egile Nagusiak: Chih-Ping Chen (Egilea), Liang-Kai Wang (Egilea), Pei-Chen Wu (Egilea), Tung-Yao Chang (Egilea), Schu-Rern Chern (Egilea), Peih-Shan Wu (Egilea), Yen-Ni Chen (Egilea), Shin-Wen Chen (Egilea), Chen-Chi Lee (Egilea), Chien-Wen Yang (Egilea), Wayseen Wang (Egilea)
• Formatua: Liburua
• Argitaratua: Elsevier, 2017-02-01T00:00:00Z.
• Gaiak: article
• Sarrera elektronikoa: Connect to this object online.

Objective: We present molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle (DORV), hypoplastic left heart syndrome (HLHS), and ductus venosus (DV) agenesis on prenatal ultrasound. Case Report: A 26-year-old woman...