Imane C. Jaouad
Rabat, Morocco
Last Updated: 09/26/2026
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Found 9 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
Mutational spectrum of BRCA1/2 genes in Moroccan patients with hereditary breast and/or ovarian cancer, and review of BRCA mutations in the MENA region.
Journal: Breast cancer research and treatment
Published: March 24, 2022
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
Application of next generation sequencing in genetic counseling a case of a couple at risk of cystinosis.
Journal: BMC medical genetics
Published: August 06, 2019
Surprisingly good outcome in antenatal diagnosis of severe hydrocephalus related to CCDC88C deficiency.
Journal: European journal of medical genetics
Published: June 14, 2017
Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature.
Journal: Gene
Published: March 28, 2017
Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene.
Journal: European journal of medical genetics
Published: September 09, 2016
Low level of consanguinity in moroccan families at high risk of breast cancer.
Journal: Asian Pacific journal of cancer prevention : APJCP
Published: April 30, 2013
Cytogenetic analysis of 5572 patients referred for suspected chromosomal abnormalities in Morocco.
Journal: Genetic testing and molecular biomarkers
Published: April 18, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026