Literature DB >> 2756579

[Consanguinity in the population of northern Tunisia].

S Riou, C el Younsi, H Chaabouni.   

Abstract

Mesh：

Year:  1989        PMID： 2756579

Source DB:  PubMed          Journal:  Tunis Med        ISSN： 0041-4131


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  11 in total

1.  Consanguinity, endogamy, and genetic disorders in Tunisia.

Authors:  Nizar Ben Halim; Nissaf Ben Alaya Bouafif; Lilia Romdhane; Rym Kefi Ben Atig; Ibtissem Chouchane; Yosra Bouyacoub; Imen Arfa; Wafa Cherif; Sonia Nouira; Faten Talmoudi; Khaled Lasram; Sana Hsouna; Welid Ghazouani; Hela Azaiez; Leila El Matri; Abdelmajid Abid; Neji Tebib; Marie-Françoise Ben Dridi; Salem Kachboura; Ahlem Amouri; Mourad Mokni; Saida Ben Arab; Koussay Dellagi; Sonia Abdelhak
Journal:  J Community Genet       Date:  2012-12-04

2.  Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia.

Authors:  R El Kares; M R Barbouche; H Elloumi-Zghal; M Bejaoui; J Chemli; F Mellouli; N Tebib; M S Abdelmoula; S Boukthir; Z Fitouri; S M'Rad; K Bouslama; H Touiri; S Abdelhak; M K Dellagi
Journal:  J Hum Genet       Date:  2006-08-26       Impact factor: 3.172

3.  Prevalence of Bardet-Biedl syndrome in Tunisia.

Authors:  Oussama M'hamdi; Ines Ouertani; Faouzi Maazoul; Habiba Chaabouni-Bouhamed
Journal:  J Community Genet       Date:  2011-02-20

4.  Glycogen storage disease type I in Tunisia: an epidemiological analysis.

Authors:  A Ben Chehida; N Tebib; W Cherif; H Ben Turkia; S Abdelmoula; H Azzouz; M F Ben Dridi
Journal:  J Inherit Metab Dis       Date:  2008-08-05       Impact factor: 4.982

5.  Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.

Authors:  Chiraz Bouchlaka; Sonia Abdelhak; Ahlem Amouri; Hela Ben Abid; Sondes Hadiji; Mounir Frikha; Tarek Ben Othman; Fethi Amri; Hammadi Ayadi; Mongia Hachicha; Ahmed Rebaï; Ali Saad; Koussay Dellagi
Journal:  J Hum Genet       Date:  2003-06-24       Impact factor: 3.172

6.  Mucopolysaccharidosis I: Alpha-L-Iduronidase mutations in three Tunisian families.

Authors:  S Laradi; T Tukel; M Erazo; J Shabbeer; L Chkioua; S Khedhiri; S Ferchichi; M Chaabouni; A Miled; R J Desnick
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.750

7.  Bleeding disorders in the tribe: result of consanguineous in breeding.

Authors:  Munira Borhany; Zaen Pahore; Zeeshan Ul Qadr; Muhammad Rehan; Arshi Naz; Asif Khan; Saqib Ansari; Tasneem Farzana; Muhammad Nadeem; Syed Amir Raza; Tahir Shamsi
Journal:  Orphanet J Rare Dis       Date:  2010-09-07       Impact factor: 4.123

8.  Consanguinity and reproductive health among Arabs.

Authors:  Ghazi O Tadmouri; Pratibha Nair; Tasneem Obeid; Mahmoud T Al Ali; Najib Al Khaja; Hanan A Hamamy
Journal:  Reprod Health       Date:  2009-10-08       Impact factor: 3.223

9.  Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East.

Authors:  Lilia Romdhane; Rym Kefi; Hela Azaiez; Nizar Ben Halim; Koussay Dellagi; Sonia Abdelhak
Journal:  Orphanet J Rare Dis       Date:  2012-08-21       Impact factor: 4.123

10.  Evidence for association of the E23K variant of KCNJ11 gene with type 2 diabetes in Tunisian population: population-based study and meta-analysis.

Authors:  Khaled Lasram; Nizar Ben Halim; Sana Hsouna; Rym Kefi; Imen Arfa; Welid Ghazouani; Henda Jamoussi; Houda Benrahma; Najla Kharrat; Ahmed Rebai; Slim Ben Ammar; Sonia Bahri; Abdelhamid Barakat; Abdelmajid Abid; Sonia Abdelhak
Journal:  Biomed Res Int       Date:  2014-07-07       Impact factor: 3.411
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