Mariam Tajir

Oujda-angad, Morocco

Last Updated: 09/26/2026

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Found 22 publications

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

Partial Trisomy of Chromosome 9 Inherited by Adjacent Segregation 2 of a Balanced Reciprocal Translocation in the Mother: Rare Mechanism in Chromosomal Abnormalities.

Journal: Balkan journal of medical genetics : BJMG

Published: November 07, 2025

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

Journal: Biomolecules & biomedicine

Published: October 25, 2025

Digital retractile keloid in a context of spontaneous keloids - a case report.

Digital retractile keloid in a context of spontaneous keloids - a case report.

Journal: Acta chirurgiae plasticae

Published: January 01, 2025

Pregnancy revealing hereditary angioedema type III with factor XII mutation managed in a resource-limited setting with no C1-inhibitor concentrate availability: a case report.

Pregnancy revealing hereditary angioedema type III with factor XII mutation managed in a resource-limited setting with no C1-inhibitor concentrate availability: a case report.

Journal: International journal of obstetric anesthesia

Published: July 25, 2024

Granulomatous Colitis Due to Hermansky-Pudlak Syndrome.

Granulomatous Colitis Due to Hermansky-Pudlak Syndrome.

Journal: ACG case reports journal

Published: January 01, 2024

Contribution of cytogenetic in the diagnosis of Edwards's syndrome: about 9 cases

Contribution of cytogenetic in the diagnosis of Edwards's syndrome: about 9 cases

Journal: Annales de biologie clinique

Published: July 21, 2023

Double Isochromosome X, a Rare Cytogenetic Variant of Turner Syndrome: A Case Report and a Review of the Literature.

Double Isochromosome X, a Rare Cytogenetic Variant of Turner Syndrome: A Case Report and a Review of the Literature.

Journal: Balkan journal of medical genetics : BJMG

Published: March 07, 2023

Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome.

Clinical description and mutational profile of a Moroccan series of patients with Rubinstein Taybi syndrome.

Journal: African health sciences

Published: November 19, 2021

Williams-Beuren syndrome: a retrospective study of a series of 11 cases at the Mohammed VI University Hospital in Marrakech

Williams-Beuren syndrome: a retrospective study of a series of 11 cases at the Mohammed VI University Hospital in Marrakech

Journal: The Pan African medical journal

Published: May 01, 2021

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.

Journal: Balkan journal of medical genetics : BJMG

Published: September 21, 2020

Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges.

Morocco's First Biobank: Establishment, Ethical Issues, Biomedical Research Opportunities, and Challenges.

Journal: BioMed research international

Published: August 26, 2020

Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco.

Patients' Knowledge and Attitude Toward Biobanks in Eastern Morocco.

Journal: Biopreservation and biobanking

Published: March 26, 2020

Showing 1-12 of 22

Last Updated: 09/26/2026