S. H. Zaidi

Mutation in the cartilage‐derived morphogenetic protein‐1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

L. Tsui, A. Teebi, W. Ahmad, 2002, Clinical genetics.

Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease.

Z. Nawaz, S. Basit, F. Al-Dayel, 2020, Cancer genetics.

Spectrum of the KIT Gene Mutations in Gastrointestinal Stromal Tumors in Arab Patients

Z. Nawaz, F. Al-Dayel, Hussah F. Alhussaini, 2018, Asian Pacific journal of cancer prevention : APJCP.

A novel HAX1 gene mutation in severe congenital neutropenia (SCN) associated with neurological manifestations

F. Al-Dayel, A. Alaiya, H. Abalkhail, 2010, European Journal of Pediatrics.

Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome

Z. Nawaz, S. Basit, A. Alsaeed, 2022, Journal of cutaneous pathology.

A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.

L. Tsui, N. Kaya, F. Al-Dayel, 2009, Atherosclerosis.

Novel and Recurrent Mutations in the C1NH Gene of Arab Patients Affected with Hereditary Angioedema

F. Al-Dayel, A. Khaliq, H. Abalkhail, 2009, International Archives of Allergy and Immunology.

Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

F. Al-Dayel, A. Cluntun, Z. Al-Hassnan, 2009, European Journal of Pediatrics.

Clinical, neuroimaging, and genetic features of L-2-hydroxyglutaric aciduria in Arab kindreds

N. Kaya, E. Faqeih, M. Rashed, 2014, Annals of Saudi medicine.