Fatima Z. Moufid
Fes, 30000, Morocco
Last Updated: 09/26/2026
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Found 9 publications
Dietary Fat Intake and KRAS Mutations in Colorectal Cancer in a Moroccan Population.
Journal: Nutrients
Published: December 04, 2021
Molecular and clinical assessment of maturity-onset diabetes of the young revealed low mutational rate in Moroccan families.
Journal: International journal of pediatrics & adolescent medicine
Published: November 30, 2020
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
Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation.
Journal: The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology
Published: October 06, 2018
The First Molecular Screening of MLH1 and MSH2 Genes in Moroccan Colorectal Cancer Patients Shows a Relatively High Mutational Prevalence.
Journal: Genetic testing and molecular biomarkers
Published: July 26, 2018
Novel NKX2-5 germline mutation in a Moroccan child with transitional atrio-ventricular septal defect (tAVSD).
Journal: The Turkish journal of pediatrics
Published: January 01, 2017
The detection of a novel insertion mutation in exon 2 of the MEFV gene associated with familial mediterranean fever in a moroccan family.
Journal: Human genome variation
Published: September 12, 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
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Last Updated: 09/26/2026