Mariam Almuriekhi

Whole exome sequencing unravels disease‐causing genes in consanguineous families in Qatar

Z. Nawaz, J. Majewski, J. Schwartzentruber, 2014, Clinical genetics.

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.

J. Al-Aama, K. Campbell, E. Dikoglu, 2016, American journal of human genetics.

Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.

Z. Nawaz, T. Shintani, M. Noda, 2015, Cell reports.

Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome

Z. Nawaz, V. Tropepe, J. Nadaf, 2015, Journal of Medical Genetics.