Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.
Research Interests

Papers共 133 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation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
Bi-allelic MED16 Variants Cause a MEDopathy with Intellectual Disability, Motor Delay, and Craniofacial, Cardiac, and Limb Malformations
Charlotte Guillouet, Valeria Agostini,Geneviève Baujat, Dario Cocciadiferro,Tommaso Pippucci,Marion Lesieur-Sebellin, Mathieu Georget,Ulrich Schatz,Christine Fauth,Raymond J Louie, Curtis Rogers, Jessica M Davis,Vassiliki Konstantopoulou,Johannes A Mayr,Arjan Bouman,Martina Wilke,Grace E VanNoy,Eleina M England, Kristen L Park, Kathleen Brown,Margarita Saenz,Antonio Novelli,Maria Cristina Digilio, Gioia Mastromoro, Mauro Ciro Antonio Rongioletti,Gerardo Piacentini,Rauan Kaiyrzhanov, Sughra Guliyeva, Lala Hasanova,Deborah Shears, Ishita Bhatnagar,Karen Stals, Oliver Klaas,Judit Horvath, University of Washington Center for Mendelian Genomics, Patrice Bouvagnet,P Dane Witmer, Gretchen MacCarrick, Katarina Cisarova,Jean-Marc Good, Svetlana Gorokhova,Odile Boute, Thomas Smol,Ange-Line Bruel,Olivier Patat, Julia R Broadbent, Tiong Y Tan, Natalie B Tan,Stanislas Lyonnet, Tiffany Busa, Claudio Graziano,Jeanne Amiel,Christopher T Gordon
American journal of human geneticsno. 4 (2025): 829-845
Cited0Views0WOSBibtex
0
0
Load More
Author Statistics

#Papers: 0

#Citation: 0

H-Index: 0

G-Index: 0

Sociability: 0

Diversity: 0

Activity: 0

  • 合作者
  • 学生
  • 导师
No result temporarily, you can search similar Scholar with the same research interest
Data Disclaimer
The page data are from open Internet sources, cooperative publishers and automatic analysis results through AI technology. We do not make any commitments and guarantees for the validity, accuracy, correctness, reliability, completeness and timeliness of the page data. If you have any questions, please contact us by email: report@aminer.cn