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-Reference-Cited by-同舟云学术

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

Published:2017-02 Issue:1 Volume:56 Page:102-105
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Chen Chih-Ping,Wang Liang-Kai,Wu Pei-Chen,Chang Tung-Yao,Chern Schu-Rern,Wu Peih-Shan,Chen Yen-Ni,Chen Shin-Wen,Lee Chen-Chi,Yang Chien-Wen,Wang Wayseen

Funder

Ministry of Science and Technology

MacKay Memorial Hospital, Taipei, Taiwan

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference30 articles.

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3. Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial cleft;Chen;Prenat Diagn,2001

4. Prenatal diagnosis of the distal 11q deletion and review of the literature;Chen;Prenat Diagn,2004

5. The 11q terminal deletion disorder: a prospective study of 110 cases;Grossfeld;Am J Med Genet,2004

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