Clinical exome sequencing in 509 Middle Eastern families with suspected Mendelian diseases: The Qatari experienceNader Al‐Dewik, Tawfeg Ben‐Omran, Fatma Al‐Mesaifri et al.|American Journal of Medical Genetics Part A|2019Cited by 57
Expanding on the phenotypic spectrum of<scp>Woodhouse‐Sakati</scp>syndrome due to founder pathogenic variant in<scp><i>DCAF17</i></scp>: Report of 58 additional patients from Qatar and literature reviewRehab Ali, Tawfeg Ben‐Omran, Nader Al‐Dewik et al.|American Journal of Medical Genetics Part A|2021Cited by 16