Deletion of CDY1b copy of Y chromosome CDY1 gene is a risk factor of male infertility in Tunisian men von Ghorbel, Myriam, Baklouti-Gargouri, Siwar, Keskes, Rim, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

Two novel mutations in COII and tRNA(His) mitochondrial genes in asthenozoospermic infertiles men von Siwar, Baklouti-Gargouri, Myriam, Ghorbel, Afif, Ben Mahmoud, Emna, Mkaouar-Rebai, Nozha, Chakroun, Afifa, Sellami, Faiza, Fakhfakh, Leila, Ammar-Keskes

Volltext

Chromosomal defects in infertile men with poor semen quality von Ghorbel, Myriam, Gargouri Baklouti, Siwar, Ben Abdallah, Fatma, Zribi, Nacira, Cherif, Mariem, Keskes, Rim, Chakroun, Nozha, Sellami, Afifa, Belguith, Neila, Kamoun, Hassen, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

A novel m.6307A>G mutation in the mitochondrial COXI gene in asthenozoospermic infertile men von Baklouti-Gargouri, Siwar, Ghorbel, Myriam, Ben Mahmoud, Afif, Mkaouar-Rebai, Emna, Cherif, Meriam, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

gr/gr-DAZ2-DAZ4-CDY1b deletion is a high-risk factor for male infertility in Tunisian population von Ghorbel, Myriam, Baklouti-Gargouri, Siwar, Keskes, Rim, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

Combined deletion of DAZ2 and DAZ4 copies of Y chromosome DAZ gene is associated with male infertility in Tunisian men von Ghorbel, Myriam, Baklouti-Gargouri, Siwar, Keskes, Rim, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

Two novel mutations in COII and tRNAHis mitochondrial genes in asthenozoospermic infertiles men von Siwar, Baklouti-Gargouri, Myriam, Ghorbel, Afif, Ben Mahmoud, Emna, Mkaouar-Rebai, Nozha, Chakroun, Afifa, Sellami, Faiza, Fakhfakh, Leila, Ammar-Keskes

Volltext

Mitochondrial DNA mutations and polymorphisms in asthenospermic infertile men von Baklouti-Gargouri, Siwar, Ghorbel, Myriam, Ben Mahmoud, Afif, Mkaouar-Rebai, Emna, Cherif, Meriam, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

Identification of a novel m.9588G > A missense mutation in the mitochondrial COIII gene in asthenozoospermic Tunisian infertile men von Baklouti-Gargouri, Siwar, Ghorbel, Myriam, Ben Mahmoud, Afif, Mkaouar-Rebai, Emna, Cherif, Meriam, Chakroun, Nozha, Sellami, Afifa, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

First functional analysis of a novel splicing mutation in the B3GALTL gene by an ex vivo approach in Tunisian patients with typical Peters plus syndrome von Ben Mahmoud, Afif, Siala, Olfa, Mansour, Riadh Ben, Driss, Fatma, Baklouti-Gargouri, Siwar, Mkaouar-Rebai, Emna, Belguith, Neila, Fakhfakh, Faiza

Volltext

Pericentric inversion of chromosom 12 [Inv (12) (p12q12)] associated with idiopathic azoospermia in one infertile Tunisian man von Ghorbel, Myriam, Baklouti-Gargouri, Siwar, ElGhazel, Hatem, Zribi, Nacira, Abdallah, Fatma Ben, Cherif, Meriem, Fakhfakh, Faiza, Saad, Ali, Ammar-Keskes, Leila

Volltext

Evaluation of the effect of c.2946+1G>T mutation on splicing in the SCN1A gene von Ben Mahmoud, Afif, Ben Mansour, Riadh, Driss, Fatma, Baklouti-Gargouri, Siwar, Siala, Olfa, Mkaouar-Rebai, Emna, Fakhfakh, Faiza

Volltext

Possible association of a novel missense mutation A6375G in the mitochondrial cytochrome C oxidase I gene with asthenospermia in the Tunisian population von Baklouti-Gargouri, Siwar, Ghorbel, Myriam, Chamkha, Imen, Mkaouar-Rebai, Emna, Sellami, Afifa, Chakroun, Nozha, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext

Partial microdeletions in the Y-chromosome AZFc region are not a significant risk factor for spermatogenic impairment in Tunisian infertile men von Ghorbel, Myriam, Gargouri, Siwar Baklouti, Zribi, Nacira, Abdallah, Fatma Ben, Cherif, Mariem, Keskes, Rim, Chakroun, Nozha, Sellami, Afifa, McElreavey, Ken, Fakhfakh, Faiza, Ammar-Keskes, Leila

Volltext