Habiba B. Chaabouni

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 11 publications

Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome.

Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome.

Journal: Steroids

Published: July 04, 2019

Fetopathological examination for the fetuses with Down syndrome in Tunisia: Epidemiological study and associated malformations.

Fetopathological examination for the fetuses with Down syndrome in Tunisia: Epidemiological study and associated malformations.

Journal: Pathology, research and practice

Published: January 07, 2017

Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family

Marshall syndrome: Clinical, radiological and genetical features of a Tunisian family

Journal: La Tunisie medicale

Published: September 15, 2015

Solid tumors after chronic lymphocytic leukemia patients: Report of six cases and review of the literature.

Solid tumors after chronic lymphocytic leukemia patients: Report of six cases and review of the literature.

Journal: The Gulf journal of oncology

Published: August 18, 2015

Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.

Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family.

Journal: Clinical genetics

Published: May 05, 2014

3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.

3-Phosphoglycerate dehydrogenase deficiency: description of two new cases in Tunisia and review of the literature.

Journal: Neuropediatrics

Published: April 09, 2013

GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.

GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.

Journal: International journal of pediatric otorhinolaryngology

Published: August 23, 2012

Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis.

Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis.

Journal: Clinical genetics

Published: August 16, 2012

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.

Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.

Journal: Journal of medical genetics

Published: July 10, 2012

Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy.

Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategy.

Journal: European journal of medical genetics

Published: February 08, 2012

Eosinophilic gastroenteritis

Eosinophilic gastroenteritis

Journal: La Revue de medecine interne

Published: October 13, 2011

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Last Updated: 09/26/2026