Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.-Reference-Cited by-同舟云学术

Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation.

Published:1996-07-01 Issue:7 Volume:33 Page:615-617
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Chen C P,Liu F F,Jan S W,Chen C P,Lan C C

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference25 articles.

1. The dup(3q) syndrome: report of eight cases and review of the literature;Steinbach, P.; WN, Jr, Adkins; Caspar, H.;Am JMed Genet,1981

2. Mendelian inheritance in man;McKusick, V.A.,1992

3. Dup3q2l --q29 in a male due to a de novo duplication inversion;Gustashaw, K.; Crowe, C.; Dickerman, L.; Golden, W.; Johnson, W.;Am _J Med Genet,1985

4. Duplication 3q(q21 -+qter) without limb anomalies;Ismail, SR, Kousseff; BG, Kotb; SM, Kholeif; S.F.;Anm 7 Med Geniet,1991

5. Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome;Rizzu, P.; Baldini, A.;Genomics,1994

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal identification of partial 3q duplication syndrome;BMC Medical Genomics;2019-06-13

2. 15q23 Gain in a Neonate with a Giant Omphalocele and Multiple Co-Occurring Anomalies;Case Reports in Pediatrics;2018-11-13

3. A girl with a 14.7 Mb 3q26.32–q28 duplication: a new report of 3q duplication syndrome and a literature review;Clinical Dysmorphology;2016-07

4. Major risk factors for stillbirth in different trimesters of pregnancy—A systematic review;Taiwanese Journal of Obstetrics and Gynecology;2014-06

5. 3q26.31–q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: Prenatal diagnosis and aCGH characterization;Gene;2013-12