Duplication and Deletion of CFC1 Associated with Heterotaxy Syndrome-Reference-Cited by-同舟云学术

Duplication and Deletion of CFC1 Associated with Heterotaxy Syndrome

Published:2015-02 Issue:2 Volume:34 Page:101-106
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Cao Ruixue¹,Long Fei²,Wang Liping¹,Xu Yuejuan²,Guo Ying³,Li Fen³,Chen Sun¹,Sun Kun¹,Xu Rang²

Affiliation:

1. Department of Pediatric Cardiology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

2. Scientific Research Center, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

3. Department of Cardiology, Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/dna.2014.2616

Reference29 articles.

1. Loss-of-function mutations in the EGF-CFC gene CFC1 are associated with human left-right laterality defects

2. Kupffer's vesicle is a ciliated organ of asymmetry in the zebrafish embryo that initiates left-right development of the brain, heart and gut

3. Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

4. X-linked situs abnormalities result from mutations in ZIC3

5. CFC1 Mutations in Patients with Transposition of the Great Arteries and Double-Outlet Right Ventricle

Cited by 7 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. Delving into the Molecular World of Single Ventricle Congenital Heart Disease;Current Cardiology Reports;2022-02-26

2. Investigating the role of EGF-CFC gene family in recurrent pregnancy loss through bioinformatics and molecular approaches;Systems Biology in Reproductive Medicine;2021-09-09

3. Identification of novel candidate genes in heterotaxy syndrome patients with congenital heart diseases by whole exome sequencing;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2020-12

4. Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia;2020-03-31

5. PhenoPro: a novel toolkit for assisting in the diagnosis of Mendelian disease;Bioinformatics;2019-02-19