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Publications by Tawfeg Ben-Omran

Inactivating Mutations in MFSD2A, Required for Omega-3 Fatty Acid Transport in Brain, Cause a Lethal Microcephaly Syndrome

Nature Genetics

English

Mutations in SCARF2 Are Responsible for Van Den Ende-Gupta Syndrome

American Journal of Human Genetics

English

Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features

American Journal of Human Genetics

English

Bi-Allelic TMEM94 Truncating Variants Are Associated With Neurodevelopmental Delay, Congenital Heart Defects, and Distinct Facial Dysmorphism

American Journal of Human Genetics

English

Clinical Application of Whole-Exome Sequencing

English

Neurodevelopmental and Cognitive Outcomes of Classical Homocystinuria: Experience From Qatar

Internal Medicine

Molecular Biology

English