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International Journal of Pediatric Otorhinolaryngology|April 2, 2018
Utility of whole exome sequencing in the diagnosis of Usher syndrome: Report of novel compound heterozygous MYO7A mutationsKhushnooda Ramzan, Mohammed Al-Owain, Rozeena Huma, et al.
Genes|December 15, 2020
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing LossKhushnooda Ramzan, Nouf S Al-Numair, Sarah Al-Ageel, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 20, 2019
Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi populationKhushnooda Ramzan, Mohammed Al-Owain, Nouf S Al-Numair, et al.
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