Imane Jaouad-Cherkaoui

Rabat, Morocco

Last Updated: 09/26/2026

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Found 10 publications

Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia.

Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia.

Journal: Hemoglobin

Published: June 04, 2024

Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report.

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

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report.

Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report.

Journal: BMC medical genomics

Published: December 14, 2020

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report.

A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report.

Journal: BMC medical genetics

Published: March 21, 2017

Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome.

Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome.

Journal: European journal of medical genetics

Published: October 19, 2016

Non lethal Raine syndrome and differential diagnosis.

Non lethal Raine syndrome and differential diagnosis.

Journal: European journal of medical genetics

Published: September 16, 2016

Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.

Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.

Journal: BMC oral health

Published: September 21, 2014

Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1 variants in Moroccan population.

Distribution of allelic and genotypic frequencies of NAT2 and CYP2E1 variants in Moroccan population.

Journal: BMC genetics

Published: May 20, 2014

Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.

Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report.

Journal: Journal of medical case reports

Published: February 22, 2014

Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family.

Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family.

Journal: European journal of medical genetics

Published: February 26, 2012

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Last Updated: 09/26/2026