Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar-Reference-Cited by-同舟云学术

Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar

Published:2013-11-10 Issue:1 Volume:35 Page:105-116
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Rodriguez-Flores Juan L.¹,Fakhro Khalid²,Hackett Neil R.¹,Salit Jacqueline¹,Fuller Jennifer¹,Agosto-Perez Francisco³,Gharbiah Maey²,Malek Joel A.²,Zirie Mahmoud⁴,Jayyousi Amin⁴,Badii Ramin⁵,Al-Nabet Al-Marri Ajayeb⁵,Chouchane Lotfi²,Stadler Dora J.⁶,Mezey Jason G.¹³,Crystal Ronald G.¹

Affiliation:

1. Department of Genetic Medicine; Weill Cornell Medical College; New York New York

2. Department of Genetic Medicine; Weill Cornell Medical College - Qatar; Doha Qatar

3. Department of Biological Statistics and Computational Biology; Cornell University; Ithaca New York

4. Department of Medicine; Hamad Medical Corporation; Doha Qatar

5. Laboratory Medicine and Pathology; Hamad Medical Corporation; Doha Qatar

6. Department of Medicine; Weill Cornell Medical College - Qatar; Doha Qatar

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference36 articles.