Aziza Sbiti

Rabat, Morocco

Last Updated: 09/26/2026

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Found 14 publications

Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome Sequencing.

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

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature.

A maternally derived complex small supernumerary marker chromosome involving chromosomes 8 and 14: case report and review of the literature.

Journal: Frontiers in genetics

Published: November 01, 2023

Currarino Syndrome in Two Moroccan Siblings with Inherited 7q36 Deletion due to Maternal t(7;21)(q36;p11)mat: A Case Report.

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

Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability.

Complex translocation leading to13q interstitial deletion in a Moroccan child with retinoblastoma and intellectual disability.

Journal: Ophthalmic genetics

Published: June 06, 2022

Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.

Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia.

Journal: The Pan African medical journal

Published: November 29, 2020

15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.

15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.

Journal: Italian journal of pediatrics

Published: June 12, 2020

Molecular diagnosis of dystrophinopathies in Morocco and report of six novel mutations.

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

Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.

Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.

Journal: Cytogenetic and genome research

Published: September 11, 2017

Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.

Cytogenetic Investigation in a Group of Ten Infertile Men with Non-Obstructive Azoospermia: First Algerian 46, XX Syndrome.

Journal: Iranian journal of public health

Published: September 21, 2016

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Journal: Journal of medical case reports

Published: January 22, 2016

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.

Journal: BMC research notes

Published: January 31, 2015

Carrier frequency of the c.525delT mutation in the SGCG gene and estimated prevalence of limb girdle muscular dystrophy type 2C among the Moroccan population.

Carrier frequency of the c.525delT mutation in the SGCG gene and estimated prevalence of limb girdle muscular dystrophy type 2C among the Moroccan population.

Journal: Genetic testing and molecular biomarkers

Published: February 21, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026