Exome Sequencing Identifies Potential Risk Variants for Mendelian Disorders at High Prevalence in Qatar
- 期刊名称Human Mutation
- 作者Rodriguez-Flores, Juan L.; Fakhro, Khalid; Hackett, Neil R.; Salit, Jacqueline; Fuller, Jennifer; Agosto-Perez, Francisco; Gharbiah, Maey; Malek, Joel A.; Zirie, Mahmoud; Jayyousi, Amin; Badii, Ramin; Al-Nabet Al-Marri, Ajayeb; Chouchane, Lotfi; Stadler, Dora J.; Mezey, Jason G.; Crystal, Ronald G.
- 卷第35卷
- 期第1期
- 印刷ISSN1059-7794
- 文件大小309.63KB
- 发表时间2014-01
- DOI10.1002/humu.22460
- 页码105-116
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