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

Comprehensive analysis of copy number variations in congenital heart defects Tunisian patients: chromosomal microarray analysis insights

对突尼斯先天性心脏病患者拷贝数变异的全面分析:染色体微阵列分析的启示

Khelifi, Rim; Othmane, Houcemeddine; Ajmi, Houda; Slimani, Wafa; Bennour, Ayda; Dardour, Leila; Soyeh, Najla; Benzarti, Amira; Rjiba, Khouloud; Abdallah, Hamza Hadj; Rassass, Ahmed; Kooli, Rim; Mghirbi, Oussama; Kammoun, Molka; Khelifa, Hela Ben; Bahri, Farouk; Hayet, Mkaddem; Ammar, Aouina; Ghanmi, Sahbi; Mathlouthi, Jihene; Ben Hamida, Hayet; Habboul, Zakia; Kemis, Tarek; Kharrat, Habib; Hassine, Nadia; Tej, Amel; Bellalah, Manel; Chouikh, Fatma; Houssine, Mejaouel; Mahdhaoui, Abdallah; Kortas, Chokri; Guith, Aida; Maatouk, Faouzi; Naffeti, Elies; Soua, Habib; Gribaa, Moez; Saad, Ali; Mougou-Zerelli, Soumaya

Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome

对泛素蛋白连接酶 E3A 基因作为安格曼综合征潜在靶点的遗传学研究

Manoubi, Wiem; Mahdouani, Marwa; Hmida, Dorra; Kdissa, Ameni; Rouissi, Aida; Turki, Ilhem; Gueddiche, Neji; Soyah, Najla; Saad, Ali; Bouwkamp, Christian; Elgersma, Ype; Mougou-Zerelli, Soumaya; Gribaa, Moez

Factors associated with anxiety and depression in men undergoing fertility investigations: a cross-sectional study

男性生育力检查中焦虑和抑郁的相关因素:一项横断面研究

Kooli, Rim; Sallem, Amira; Chebil, Dhekra; Boussabbeh, Manel; Mohamed, Bochra Ben; Ajina, Tesnim; Boughzela, Ines; Mougou, Soumaya; Mehdi, Meriem

Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis

人类性别决定异常:联合细胞遗传学方法在鉴定一例伴有46,XY性腺发育不全的Xp功能性二体病例中的应用价值

Rjiba, Khouloud; Slimani, Wafa; Gaddas, Meriem; Hassine, Ikbel Hadj; Jelloul, Afef; Khelifa, Hela Ben; El Amri, Fethi; Zaouali, Monia; Mcelreavey, Kenneth; Saad, Ali; Mougou-Zerelli, Soumaya

Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development

染色体不平衡以及SOX8、ZNRF3和HHAT基因变异在人类早期睾丸发育中的作用的更多证据

Rjiba, Khouloud; Mougou-Zerelli, Soumaya; Hamida, Imen Hadj; Saad, Ghada; Khadija, Bochra; Jelloul, Afef; Slimani, Wafa; Hasni, Yosra; Dimassi, Sarra; Khelifa, Hela Ben; Sallem, Amira; Kammoun, Molka; Abdallah, Hamza Hadj; Gribaa, Moez; Bignon-Topalovic, Joelle; Chelly, Sami; Khairi, Hédi; Bibi, Mohamed; Kacem, Maha; Saad, Ali; Bashamboo, Anu; McElreavey, Kenneth

Detection of Maternal and Cytoplasmic Effects on Resistance to Zymoseptoria tritici in Durum Wheat

检测母体和细胞质效应对硬粒小麦抗小麦颖枯病菌的影响

Hassine, Marwa; Bnejdi, Fethi; Bahri, Bochra Amina; Tissaoui, Salma; Mougou-Hamdane, Amira; Guesmi, Mouna; Baraket, Mokhtar; Slim-Amara, Hajer

Varietal Screening of Durum Wheat Varieties for Resistance to Pyrenophora tritici-repentis (Tan Spot) under Field Conditions

田间条件下硬粒小麦品种抗小麦褐斑病菌(Pyrenophora tritici-repentis)的品种筛选

Tissaoui, Salma; Hassine, Marwa; Mougou-Hamdane, Amira; Araar, Ala Eddine Ben; Nasraoui, Romdhane; Nasraoui, Bouzid

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review

1q43q44缺失和胼胝体畸形的临床和分子特征:2例新病例报告及文献综述

Khadija, Bochra; Rjiba, Khouloud; Dimassi, Sarra; Dahleb, Wafa; Kammoun, Molka; Hannechi, Hanen; Miladi, Najoua; Gouider-Khouja, Neziha; Saad, Ali; Mougou-Zerelli, Soumaya

Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay-Does both possibly act to modulate a candidate gene region for the patient's phenotype?

病例报告:一名患有癫痫和精神运动发育迟缓的患者存在 7p22.3 缺失和 8q24.3 重复——两者是否有可能调节患者表型的候选基因区域?

Touhami, Rahma; Foddha, Hajer; Alix, Eudeline; Jalloul, Afef; Mougou-Zerelli, Soumaya; Saad, Ali; Sanlaville, Damien; Haj Khelil, Amel

Bacillus velezensis strain MBY2, a potential agent for the management of crown gall disease

贝莱斯芽孢杆菌MBY2菌株,一种潜在的冠瘿病防治剂

Ben Gharsa, Haifa; Bouri, Meriam; Mougou Hamdane, Amira; Schuster, Christina; Leclerque, Andreas; Rhouma, Ali