Faisal Almalki

2PUBLICATIONS
1CO-AUTHORS
Gene mappingNeurogenetics
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Publications (2)

|Aug 27, 2025
A Novel Homozygous Splice Variant in the NUP188 Gene Causing Sandestig-Stefanova Syndrome in a Saudi Patient.

Faisal Almalki, Haifa Abdullah Alkorbi, Naglaa M Kamal

|Mar 22, 2024
Review and research gap identification in genetics causes of syndromic and nonsyndromic hearing loss in Saudi Arabia.

Faisal Almalki

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Frequent Collaborators

1 joint publications

Jwaher Mesleh Althobiti