Imane Samri
Fes, Morocco
Last Updated: 09/26/2026
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Found 10 publications
Absence of GATA4 Mutations in Moroccan Patients with Atrial Septal Defect (ASD) Provides Further Evidence of Limited Involvement of GATA4 in Major Congenital Heart Defects.
Journal: The Eurasian journal of medicine
Published: November 19, 2020
GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
Journal: African health sciences
Published: February 16, 2019
NKX2-5 molecular screening and assessment of variant rate and risk factors of secundum atrial septal defect in a Moroccan population.
Journal: Anatolian journal of cardiology
Published: October 19, 2016
Noonan syndrome-causing genes: Molecular update and an assessment of the mutation rate.
Journal: International journal of pediatrics & adolescent medicine
Published: April 15, 2016
The first PTPN1 1 mutations in hotspot exons reported in Moroccan children with Noonan syndrome and comparison of mutation rate to previous studies.
Journal: Turkish journal of medical sciences
Published: June 19, 2015
TPMT alleles in the Moroccans.
Journal: Clinics and research in hepatology and gastroenterology
Published: October 10, 2014
Lynch syndrome: case report and review of the literature
Journal: The Pan African medical journal
Published: April 16, 2014
Fanconi anemia at the University Hospital (CHU) Hassan II of Fez: about 6 cases
Journal: The Pan African medical journal
Published: April 13, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026