Human Genome Epidemiology Literature Finder
|
Records 1 - 4 (of 4 Records) |
| Query Trace: Heart Diseases and TBX5[original query] |
|---|
| TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy. Biochemical and biophysical research communications 2015 Mar 459 (1): 166-71. Zhang Xian-Ling, Qiu Xing-Biao, Yuan Fang, Wang Juan, Zhao Cui-Mei, Li Ruo-Gu, Xu Lei, Xu Ying-Jia, Shi Hong-Yu, Hou Xu-Min, Qu Xin-Kai, Xu Ya-Wei, Yang Yi-Qi |
| Gerbode Ventricular Septal Defect -A Rare Cardiac Anomaly Associated with Genetic Variants in Indian Population- A Case Series. Journal of clinical and diagnostic research : JCDR 2017 Mar 11 (3): GR01-GR04. Borkar Yashvanthi, Nayak Krishnananda, Shetty Ranjan K, Bhat Gopalakrishna, Moka Rajasekh |
| Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects. Journal of cardiovascular and thoracic research 2018 5 10 (1): 41-45. Khatami Mehri, Heidari Mohammad Mehdi, Kazeminasab Fatemeh, Zare Bidaki Razi |
| Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children. Molecular genetics & genomic medicine 2019 Mar e612. Behiry Eman G, Al-Azzouny Mahmoud A, Sabry Dina, Behairy Ola G, Salem Nessrine |
- Page last reviewed:Feb 1, 2024
- Content source: