日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genetics of prelingual isolated deafness and Usher syndrome in the Maghreb and Jordan: Harnessing the potential of homozygosity

马格里布和约旦语前孤立性耳聋和厄舍尔综合征的遗传学:利用纯合子的潜力

Riahi, Zied; Boucher, Sophie; Abdi, Samia; Wong Jun Tai, Fabienne; Singh-Estivalet, Amrit; Aghaie, Asadollah; Niasme-Grare, Magali; Hardelin, Jean-Pierre; Behlouli, Asma; Dahmani, Malika; Talbi, Sonia; Bouyacoub, Yosra; Mkaouar, Rahma; Charfeddine, Cherine; Amalou, Ghita; Bakhchane, Amina; Bousfiha, Amale; Salime, Sara; Elrharchi, Soukaina; Salame, Malak; Hadrami, Mouna; Boussaty, Ely; Charoute, Hicham; Detsouli, Mustapha; Snoussi, Khalid; Rouba, Hassan; Hachmi, Hala El; Veten, Fatimetou; Meiloud, Ghlana; Marrakchi, Jihene; Zainine, Rim; Chahed, Houda; Besbes, Ghazi; Trabelsi, Mediha; Mrad, Ridha; Kraoua, Ichraf; Ouhab, Sofiane; Djennaoui, Djamel; Boudjenah, Farid; Chouery, Eliane; Mustapha, Mirna; Houmeida, Ahmed; Barakat, Abdelhamid; Khodja, Fatima Ammar; Makrelouf, Mohamed; Zenati, Akila; Beltaief, Najeh; Abdelhak, Sonia; Petit, Christine; Bonnet, Crystel

Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

更正:突尼斯综合征性耳聋的当前表型和遗传谱:为精准听觉健康铺平道路

Mkaouar, Rahma; Riahi, Zied; Marrakchi, Jihene; Mezzi, Nessrine; Romdhane, Lilia; Boujemaa, Maroua; Dallali, Hamza; Sayeb, Marwa; Lahbib, Saida; Jaouadi, Hajer; Boudabbous, Hela; Zekri, Lotfi; Chargui, Mariem; Messaoud, Olfa; Elyounsi, Meriem; Kraoua, Ichraf; Zaouak, Anissa; Turki, Ilhem; Mokni, Mourad; Boucher, Sophie; Petit, Christine; Giraudet, Fabrice; Mbarek, Chiraz; Besbes, Ghazi; Halayem, Soumeyya; Zainine, Rim; Turki, Hamida; Tounsi, Amel; Bonnet, Crystel; Mrad, Ridha; Abdelhak, Sonia; Trabelsi, Mediha; Charfeddine, Cherine

Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health

突尼斯综合征性耳聋的当前表型和遗传谱:为精准听觉健康铺平道路

Mkaouar, Rahma; Riahi, Zied; Marrakchi, Jihene; Mezzi, Nessrine; Romdhane, Lilia; Boujemaa, Maroua; Dallali, Hamza; Sayeb, Marwa; Lahbib, Saida; Jaouadi, Hager; Boudabbous, Hela; Zekri, Lotfi; Chargui, Mariem; Messaoud, Olfa; Elyounsi, Meriem; Kraoua, Ichraf; Zaouak, Anissa; Turki, Ilhem; Mokni, Mourad; Boucher, Sophie; Petit, Christine; Giraudet, Fabrice; Mbarek, Chiraz; Besbes, Ghazi; Halayem, Soumeyya; Zainine, Rim; Turki, Hamida; Tounsi, Amel; Bonnet, Crystel; Mrad, Ridha; Abdelhak, Sonia; Trabelsi, Mediha; Charfeddine, Cherine

Ludwig's Angina

路德维希氏心绞痛

Chaabouni, Hela; Bechraoui, Rim; Kriaa, Maamoun; Zainine, Rim; Besbes, Ghazi

Whole exome sequencing identifies mutations in Usher syndrome genes in profoundly deaf Tunisian patients

全外显子组测序在重度耳聋的突尼斯患者中发现了 Usher 综合征基因突变

Riahi, Zied; Bonnet, Crystel; Zainine, Rim; Lahbib, Saida; Bouyacoub, Yosra; Bechraoui, Rym; Marrakchi, Jihène; Hardelin, Jean-Pierre; Louha, Malek; Largueche, Leila; Ben Yahia, Salim; Kheirallah, Moncef; Elmatri, Leila; Besbes, Ghazi; Abdelhak, Sonia; Petit, Christine