Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Mariam Almureikhi

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

American Journal of Human Genetics

English

Related publications

Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 De Novo Deletion in a Patient With Van Den Ende-Gupta Syndrome

Molecular Syndromology

English

Two Novel Mutations Confirm FGD1 Is Responsible for the Aarskog Syndrome

European Journal of Human Genetics

English

Integrin Alpha 8 Recessive Mutations Are Responsible for Bilateral Renal Agenesis in Humans

American Journal of Human Genetics

English

Mutations in the PCYT1A Gene Are Responsible for Isolated Forms of Retinal Dystrophy

European Journal of Human Genetics

English

Two Novel Nonsense Mutations in GALNT3 Gene Are Responsible for Familial Tumoral Calcinosis

Journal of Human Genetics

English

Amerika Nach Den „Midterms“ – Anfang Vom Ende Oder Ende Des Anfangs Der Trump-Ära?

GWP – Gesellschaft, Wirtschaft, Politik

English

Ellis-Van Creveld Syndrome: Mutations Uncovered in Lebanese Families

Case Reports in Genetics

English

Novel IRF6 Mutations in Honduran Van Der Woude Syndrome Patients

Molecular Medicine Reports

Molecular Biology

Cancer Research

Molecular Medicine

English

De Taak Van Den Accountant Ten Opzichte Van De Opname Van Den Goederenvoorraad

Maandblad Voor Accountancy en Bedrijfseconomie

English