Saeed Al Tala

Molecular autopsy in maternal–fetal medicine

F. Alkuraya, E. Faqeih, T. Ben-Omran, 2017, Genetics in Medicine.

Mutations of the Histone Linker H1-4: An Expanded Cohort and Functional Characterization of Frameshift Mutant H1.4 in Neurons

J. Rosenfeld, W. Craigen, A. West, 2020 .

Genomic and phenotypic delineation of congenital microcephaly

C. Walsh, F. Alkuraya, S. Arold, 2018, Genetics in Medicine.

Mutations in DONSON disrupt replication fork stability and cause microcephalic 1 dwarfism . 2 3

Martin A. M. Reijns, Saleem, Abdulrahman, 2017 .

Biallelic pathogenic variants in COX11 are associated with an infantile‐onset mitochondrial encephalopathy

Neal K. Bennett, M. Cowley, J. Christodoulou, 2022, Human Mutation.

Genomic and phenotypic delineation of congenital microcephaly

C. Walsh, F. Alkuraya, S. Arold, 2018, Genetics in Medicine.

Expanding the phenome and variome of skeletal dysplasia

S. Kapoor, F. Alkuraya, E. Faqeih, 2018, Genetics in Medicine.