Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype-Reference-Cited by-同舟云学术

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Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype

Published:2010-12-01 Issue:4 Volume:11 Page:228-232
ISSN:1309-0399
Container-title:Journal of the Turkish German Gynecological Association
language:
Short-container-title:J Turkish German Gynecol Assoc

Author:

Arikan Deniz Cemgil,Coskun Ayhan,Arikan Ilker,Kiran Gurkan,Ceylaner Gulay

Publisher

Galenos Yayinevi

Subject

Obstetrics and Gynaecology

Link

http://cms.galenos.com.tr/FileIssue/27/1060/article/JTGGA_11_4_228_232.pdf

Cited by 5 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. New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception;Italian Journal of Pediatrics;2023-02-09

2. Approach to inherited hypertrichosis: A brief review;Indian Journal of Dermatology, Venereology and Leprology;2021-07-29

3. Inherited unbalanced reciprocal translocation with 3q duplication and 5p deletion in a foetus revealed by cell-free foetal DNA (cffDNA) testing: a case report;European Journal of Medical Research;2021-06-29

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

5. Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family;Molecular Cytogenetics;2018-02-20

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