Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot-Reference-Cited by-同舟云学术

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot

Published:2016-04 Issue:2 Volume:55 Page:270-274
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,Chen Chen-Yu,Chern Schu-Rern,Wu Peih-Shan,Chen Yen-Ni,Chen Shin-Wen,Chen Li-Feng,Yang Chien-Wen,Wang Wayseen

Funder

Ministry of Science and Technology

MacKay Memorial Hospital

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology

Reference25 articles.

1. Chromosome 6/15 translocation with multiple congenital anomalies;Ming;Obstet Gynecol,1977

2. The Prader–Willi syndrome with a 15/3 translocation;Kucerova;J Med Genet,1979

3. Congenital heart disease with del(15q) mosaicism;Herva;Clin Genet,1980

4. Adjacent 2 meiotic disjunction. report of a case resulting from a familial 13q;15q balanced reciprocal translocation and review of the literature;Duckett;Hum Genet,1981

5. 'Expanded' Prader–Willi syndrome in a boy with an unusual 15q chromosome deletion;Pauli;Am J Dis Child,1983

Cited by 6 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 diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader–Willi syndrome;Taiwanese Journal of Obstetrics and Gynecology;2021-03

2. Neural crest cells require Meis2 for patterning the mandibular arch via the Sonic hedgehog pathway;Biology Open;2020-06-15

3. A long noncoding RNA cluster-based genomic locus maintains proper development and visual function;Nucleic Acids Research;2019-05-25

4. Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disability;European Journal of Human Genetics;2018-10-05

5. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA , CELF4 and SETBP1;Taiwanese Journal of Obstetrics and Gynecology;2017-12