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Details for article 13 of 52 found articles
| Title: |
Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease |
| Author: |
Teekakirikul, Polakit Zhu, Wenjuan Gabriel, George C. Young, Cullen B. Williams, Kylia Martin, Lisa J. Hill, Jennifer C. Richards, Tara Billaud, Marie Phillippi, Julie A. Wang, Jianbin Wu, Yijen Tan, Tuantuan Devine, William Lin, Jiuann-huey Bais, Abha S. Klonowski, Jonathan de Bellaing, Anne Moreau Saini, Ankur Wang, Michael X. Emerel, Leonid Salamacha, Nathan Wyman, Samuel K. Lee, Carrie Li, Hung Sing Miron, Anastasia Zhang, Jingyu Xing, Jianhua McNamara, Dennis M. Fung, Erik Kirshbom, Paul Mahle, William Kochilas, Lazaros K. He, Yihua Garg, Vidu White, Peter McBride, Kim L. Benson, D. Woodrow Gleason, Thomas G. Mital, Seema Lo, Cecilia W. |
| Appeared in: |
Human genetics and genomics advances |
| Paging: | Volume 2 () nr. 3 pages p. |
| Year: |
2021 |
| Contents: | |
| Publisher: |
The Authors |
| Source file: |
Elektronische Wetenschappelijke Tijdschriften |
Details for article 13 of 52 found articles
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