Habiba Chaabouni Bouhamed

Habiba Chaabouni Bouhamed

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Habiba Chaabouni Bouhamed

Habiba Chaabouni Bouhamed

Publications by authors named "Habiba Chaabouni Bouhamed"

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16Publications

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Genetics and genomic medicine in Tunisia.

Mol Genet Genomic Med 2018 03;6(2):134-159

University Tunis El Manar, Tunis, Tunisia.

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http://doi.wiley.com/10.1002/mgg3.392
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http://dx.doi.org/10.1002/mgg3.392DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902400PMC
March 2018

Family history predictors of BRCA1/BRCA2 mutation status among Tunisian breast/ovarian cancer families.

Breast Cancer 2017 Mar 30;24(2):238-244. Epub 2016 Mar 30.

Department of Hereditary and Congenital Disorders, Charles Nicolle Hospital, Tunis, Tunisia.

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http://dx.doi.org/10.1007/s12282-016-0693-4DOI Listing
March 2017

Estimating the Total Pathogenic Allele Frequency of Autosomal Recessive Disorders in Case of Consanguinity.

Hum Hered 2015 6;80(2):69-78. Epub 2015 Nov 6.

Department of Epidemiology and Biostatistics, VU University Medical Center, Amsterdam, The Netherlands.

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https://www.karger.com/Article/FullText/438862
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http://dx.doi.org/10.1159/000438862DOI Listing
September 2016

Molecular analysis of the PAX6 gene for aniridia and congenital cataracts in Tunisian families.

Hum Genome Var 2014 4;1:14008. Epub 2014 Sep 4.

Faculté de Médecine de Tunis, Laboratoire Génétique Humaine, Tunis, Tunisia; Charles Nicolle Hospital, Congenital and Hereditary Disorders Department, Tunis, Tunisia.

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http://dx.doi.org/10.1038/hgv.2014.8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785518PMC
April 2016

CONSANGUINITY AND HOMOZYGOSITY AMONG TUNISIAN PATIENTS WITH AN AUTOSOMAL RECESSIVE DISORDER.

J Biosoc Sci 2015 Nov 29;47(6):718-26. Epub 2015 Jan 29.

*Laboratory of Human Genetics, Faculty of Medicine of Tunis,University of Tunis El Manar,Tunis,Tunisia.

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http://dx.doi.org/10.1017/S002193201400056XDOI Listing
November 2015

High-resolution melting (HRM) assay for the detection of recurrent BRCA1/BRCA2 germline mutations in Tunisian breast/ovarian cancer families.

Fam Cancer 2014 Dec;13(4):603-9

Laboratoire Génétique Humaine, Faculté de Médecine de Tunis, University Tunis El Manar, Tunis, Tunisia.

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http://link.springer.com/10.1007/s10689-014-9740-5
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http://dx.doi.org/10.1007/s10689-014-9740-5DOI Listing
December 2014

RGS6: a novel gene associated with congenital cataract, mental retardation, and microcephaly in a Tunisian family.

Invest Ophthalmol Vis Sci 2014 Dec 18;56(2):1261-6. Epub 2014 Dec 18.

Laboratoire Génétique Humaine, Faculté Médecine de Tunis, University Tunis El Manar, Tunis, Tunisia Charles Nicolle Hospital, Congenital and Hereditary Disorders Department, Tunis, Tunisia.

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http://dx.doi.org/10.1167/iovs.14-15198DOI Listing
December 2014

Prevalence of Bardet-Biedl syndrome in Tunisia.

J Community Genet 2011 Jun 20;2(2):97-9. Epub 2011 Feb 20.

Faculté de Médecine de Tunis, University Tunis el Manar, Tunis, Tunisia.

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http://dx.doi.org/10.1007/s12687-011-0040-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3186025PMC
June 2011

Non-syndromic autosomal recessive mental retardation in Tunisian families : exclusion of GRIK2 and TUSC3 genes.

Tunis Med 2011 May;89(5):479-84

Laboratoire de Genetique Humaine de la faculte de medecine de Tunis, La Rabta, Tunis.

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May 2011

Absence of PITX3 mutation in a Tunisian family with congenital cataract and mental retardation.

Mol Vis 2010 Apr 3;16:582-5. Epub 2010 Apr 3.

Faculté de Médecine de Tunis, Laboratoire Génétique Humaine, Tunis, Tunisia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848917PMC
April 2010

Tunisia: communities and community genetics.

Community Genet 2008 5;11(6):313-23. Epub 2008 Aug 5.

Department of Hereditary Disorders, Charles Nicolle Hospital, Human Genetics Laboratory, Medical School of Tunis, Tunis, Tunisia.

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http://dx.doi.org/10.1159/000133303DOI Listing
November 2008