1. Whole exome sequencing enables the correct diagnosis of Frank–Ter Haar syndrome in a Saudi family
   Y. N. Khan et al, 2024, Vavilov Journal of Genetics and Breeding CrossRef
2. Screening of ACTN4 and PLCE1 Genes Mutations in Saudi Children Patients with Steroid Resistant Nephrotic Syndrome
   Ahmed Gaber et al, 2020, Pakistan Journal of Biological Sciences CrossRef
3. Genetic diagnosis of a rare COL7A1 variant causing dystrophic epidermolysis bullosa pruriginosa through whole‑exome sequencing
   Yanhui Yang et al, 2023, Experimental and Therapeutic Medicine CrossRef
4. A novel missense variant in the RASGRP2 gene in patients with moderate to severe bleeding disorder
   Essa Alharby et al, 2020, Platelets CrossRef