Hadil Alrohaif
Kuwait City, KU, Kuwait
Last Updated: 09/26/2026
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Found 8 publications
Identification of Novel and Rare Gene Variants in Cleft Lip/Palate Patients From Kuwaiti Consanguineous Families by Exome Sequencing.
Journal: American journal of medical genetics. Part A
Published: March 19, 2025
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD.
Journal: Brain : a journal of neurology
Published: June 08, 2024
Variants in WASHC3, a component of the WASH complex, cause short stature, variable neurodevelopmental abnormalities, and distinctive facial dysmorphism.
Journal: Genetics in medicine open
Published: May 22, 2024
Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects.
Journal: Brain : a journal of neurology
Published: October 03, 2022
Case Report: The Genetic Diagnosis of Duchenne Muscular Dystrophy in the Middle East.
Journal: Frontiers in pediatrics
Published: May 28, 2021
GNE myopathy in the bedouin population of Kuwait: Genetics, prevalence, and clinical description.
Journal: Muscle & nerve
Published: January 31, 2018
Whole-exome sequencing identifies mutations in MYMK in a mild form of Carey-Fineman-Ziter syndrome.
Journal: Neurology. Genetics
Published: November 30, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026