Bayen MaalejPediat Dept Hedi Chaker Hosp关注立即认领分享关注立即认领分享基本信息浏览量:0职业迁徙个人简介暂无内容研究兴趣论文共 2 篇作者统计合作学者相似作者按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选时间引用量主题期刊级别合作者合作机构Custom Next-Generation Sequencing Identifies Novel Mutations Expanding the Molecular and clinical spectrum of isolated Hearing Impairment or along with defects of the retina, the thyroid, and the kidneysMariem Ben Said,Ikhlas Ben Ayed,Ines Elloumi,Mehdi Hasnaoui,Amal Souissi,Nabil Idriss,Hajer Aloulou,Imen Chabchoub,Bayen Maâlej,Dorra Driss,Saber MasmoudiMOLECULAR GENETICS & GENOMIC MEDICINE(2022)引用2浏览0WOS引用20Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients Sawssan Ammar,Houda Kanoun,Khawla Kammoun,Andrea Domingo-Gallego,Patricia Ruiz,Laura Lorente-Grandoso,Marc Pybus,Bayen Maalej,Tahya Boudawara,Hassen Kamoun,Mohamed Ben Hmida,Elisabet Ars,JOURNAL OF HUMAN GENETICS(2021)引用6浏览0WOSNATURE引用60作者统计合作学者合作机构D-Core合作者学生导师暂无相似学者,你可以通过学者研究领域进行搜索筛选数据免责声明页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果,我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问,可以通过电子邮件方式联系我们:report@aminer.cn