Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis-Reference-Cited by-同舟云学术

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Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis

Published:2013-12 Issue:4 Volume:52 Page:602-606
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Sung Pi-Lin,Cheng Eong-Eong,Chen Yann-Jang,Chern Schu-Rern,Shih Chung-Yu,Chang Chia-Ming,Wang Peng-Hui,Yen Ming-Shyen,Huang Chi-Ying F.,Chen Chih-Ping

Funder

Yen Tjing Ling Medical Foundation

Taipei Veterans General Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference28 articles.

2. Tentative localization of a Hageman (Factor XII) locus on 7q, probably the 7q35 band;de Grouchy;Humangenetik,1974

3. 7q deletion syndrome (7q32 leads to 7qter);Harris;Clin Genet,1977

4. A partial long arm deletion of chromosome 7:46, XY, del(7)(q32);Kousseff;J Med Genet,1977

5. Balanced t(8;9)(q12;q33)pat carrier with phenotypic abnormalities attributable to a de novo terminal deletion of the long arm of chromosome 7;Biederman;Hum Genet,1978

Cited by 1 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. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature;Taiwanese Journal of Obstetrics and Gynecology;2015-06

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