Maryem Sahli
Rabat, Morocco
Last Updated: 09/26/2026
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Found 11 publications
Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome Sequencing.
Journal: Molecular genetics & genomic medicine
Published: September 11, 2025
Clinical Exome Sequencing as a Key Diagnostic Tool: A Rare de novo TRIO Variant in Dizygotic Twins.
Journal: Molecular syndromology
Published: July 17, 2025
Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.
Journal: Molecular syndromology
Published: May 18, 2023
Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report.
Journal: Journal of medical case reports
Published: February 18, 2023
Salmonella thyroid abscess.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: May 31, 2021
Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: November 05, 2019
Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series.
Journal: Journal of medical case reports
Published: March 29, 2019
Post-mortem diagnosis of Pompe disease by exome sequencing in a Moroccan family: a case report.
Journal: Journal of medical case reports
Published: February 19, 2018
Hamartoma of the tongue.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: July 03, 2017
Laryngeal involvement of rhinoscleroma.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: September 06, 2015
Nasopharyngeal branchial cyst.
Journal: European annals of otorhinolaryngology, head and neck diseases
Published: December 03, 2013
Showing 1-11 of 11
Last Updated: 09/26/2026