Khushnooda Ramzan
0000-0002-0234-4996
King Faisal Specialist Hospital & Research Centre
3 papers found
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Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss
Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population
Evidence for an autosomal recessive pattern of inheritance in Keratitis-ichthyosis-deafness (KID) syndrome: Exome sequencing reveals a novel homozygous GJB2 mutation
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