Genetics

All Items

• Marfan syndrome in a Triple-X girl: a new association?

  Faten Tinsa, Lotfi Karboul, Jalel Chekib, samia Hamouda, Lamia Ben Jemaa, Khadija Boussetta, Souad Bousnina

• Phenotype and mutational spectrum in Tunisian pediatric gaucher disease

  Hadhami Ben Turkia, Imen Riahi, Hatem Azzouz, Saloua Ladab, Wafa Cherif, Amal Ben Chehida, Mohamed S. Abdelmoula, Catherine Caillaud, Jalel Chemli, Sonia Abdelhak, Neji Tebib, Marie F. Ben Dridi

• Recessive autosomic polycystic kidney in a Tunisian family: correlation between genotype and phenotype?

  F TINSA, S YAHYAOUI, I BRINI, L MICHEL-CALEMARD, K BOUSSETTA, S BOUSNINA

• PENETRANCE OF BRCA1 GENE MUTATION AND DNA MITOCHONDRIAL IN TUNISIAN BREAST CANCER OCCURRENCE

  Wafa Troudi, Besma Loueslati, Amal Baccar, Farhat Ben Ayed, Amel Ben Ammar El Gaaied

• X LINKED MENTAL RETARDATION

  Imen Rejeb, Lamia Ben Jemaa, Habiba Chaabouni

• ARE HLA DQB1 ALLELES CORRELATED WITH BREAST CANCER HISTOPRONOSTIC PARAMETERS IN TUNISIA?

  Amal Baccar, Besma Yacoubi Loueslati, Wafa Troudi, Slama Hmida, Amel Dridi, Afef Jridi, Karima Mrad, Khaled Ben Romdhane, Amel Ben Ammar Elgaaied