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排名必读论文期刊顶会热点AI 简史溯源树小脉星探人才迁徙塔尖人才国防情报追踪开源工具智慧手语
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论文共 55 篇作者统计合作学者相似作者

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Clinical and genetic characteristics of carriers of the TP53 c.541C > T, p.Arg181Cys pathogenic variant causing hereditary cancer in patients of Arab-Muslim descent
Johnathan Arnon,Aviad Zick,Myriam Maoz, Nada Salaymeh, Ahinoam Gugenheim, MazalTov Marouani, Eden Mor,Tamar Hamburger, Nagam Saadi, Anna Elia, Gael Ganz,Duha Fahham,
Familial Cancerpp.1-12, (2024)
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A Case Report of Familial Mayer-Rokitansky-Kuster-Hauser Syndrome as Part of the Phenotypic Spectrum of the 2q37 Deletion
Hagit Daum, Einav Kremer,Ayala Frumkin,Vardiella Meiner, Hagit Diamant, Iris Harel,Dvora Bauman
JOURNAL OF PEDIATRIC AND ADOLESCENT GYNECOLOGYno. 1 (2024): 95-97
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Variable clinical expression of a novel FLNC truncating variant in a large family
Orr Tomer, Smadar Horowitz-Cederboim, Dini Rivkin,Vardiella Meiner,Michael H. Gollob,Donna R. Zwas,Ronen Durst,Ayelet Shauer
INTERNATIONAL JOURNAL OF CARDIOLOGY (2024): 131849-131849
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The number of non-pathogenic CNVs impacts the risk of preterm birth
Michal Macarov, Tal Bamberger,Naama Elefant,Hanah Margalit,Ayala Frumkin,Shamir Zenvirt,Vardiella Meiner, Shiri Shkedi Rafid,Hagit Hochner
EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 102-103
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Novel RAB39B Mutation Causes Parkinsonism in Males with Developmental Disorder
Roy Dayan, Shiri Shkedi Rafid,Halen Baker Erdman,Caroline Weill, Avraham Shag,Vardiella Meiner,David Arkadir
MOVEMENT DISORDERS CLINICAL PRACTICEno. 3 (2024): 306-308
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A novel rare pathogenic variant in TLN1 in a family with systemic capillary leak syndrome
Naama Elefant,Shira Yanovsky-Dagan, Danit Oz-Levi, Racheli Sion-Sarid,Doron Lancet,Vardiella Meiner, Ben Goult, Vasso Kostourou,Tamar Harel
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 411-411
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Vhl-Related Neuroendocrine Neoplasms And Beyond: An Israeli Specialized Center Real-Life Report
A Szalat,K Oleinikov, A Nahmias,V Meiner,S Ben-Haim, K Atlan, N Lev-Cohain, L Appelbaum, J M Gomori, H Mazeh, A Khalaileh, J Pe'er,
ENDOCRINE PRACTICE（2020）
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