E. Mardawi

Molecular autopsy in maternal–fetal medicine

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

Genomic analysis of Meckel–Gruber syndrome in Arabs reveals marked genetic heterogeneity and novel candidate genes

F. Alkuraya, C. Farra, E. Faqeih, 2012, European Journal of Human Genetics.

Rudimentary Uterine Horn Pregnancy; Pre-rupture Diagnosis and Management: Case Report

E. Mardawi, Ahmad Talal Chamsi, R. Bahyan, 2019 .

Mutations in TMEM231 cause Meckel–Gruber syndrome

F. Alkuraya, R. Shaheen, M. Alshammari, 2013, Journal of Medical Genetics.

Beyond the exome: utility of long-read whole genome sequencing in exome-negative autosomal recessive diseases

F. Alkuraya, E. Faqeih, K. Khabar, 2023, Genome medicine.