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RAD21 mutations cause a human cohesinopathy
Matthew A. Deardorff*, Jonathan J. Wilde, Melanie Albrecht, Emma Dickinson, Stephanie Tennstedt, Diana Braunholz, Maren Mönnich, Yuqian Yan, Weizhen Xu, María Concepcion Gil-Rodríguez, Dinah Clark, Hakon Hakonarson, Sara Halbach, Laura Daniela Michelis, Abhinav Rampuria, Eva Rossier, Stephanie Spranger, Lionel Van Maldergem, Sally Ann Lynch, Gabriele Gillessen-Kaesbach
*Corresponding author for this work
- Division of Genetics
- University of Pennsylvania
- Perelman School of Medicine
- Department of Pathology
- Dunedin School of Medicine
- Research Division
- Peter Maccallum Cancer Centre
- Zhejiang University
- Unit of Clinical Genetics and Functional Genomics
- University of Zaragoza
- University of Chicago
- Genetikum
- Praxis für Humangenetik
- Centre de Génétique Humaine
- Université de Franche-Comté
- Our Lady's Children's Hospital
- National Centre for Medical Genetics
- Institut für Humangenetik
- University of Duisburg-Essen
- Sir Peter MacCallum Department of Oncology
- University of Melbourne
- North Coast Cancer Institute
- University of Sydney
119
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(Scopus)