首页 | 本学科首页   官方微博 | 高级检索  
     


Stepwise partitioning of Xp21: a profiling method for XK deletions causative of the McLeod syndrome
Authors:Christoph Gassner  Chantal Brönnimann  Yvonne Merki  Maja P. Mattle‐Greminger  Sonja Sigurdardottir  Eduardo Meyer  Charlotte Engström  John D. O'Sullivan  Hans H. Jung  Beat M. Frey
Affiliation:1. Department of Molecular Diagnostics & Research (MOC), Swiss Red Cross (SRC), Zürich‐Schlieren, Switzerland;2. Department of Quality Control and FACS Analysis, Swiss Red Cross (SRC), Zürich‐Schlieren, Switzerland;3. Department of Immunohematology, Swiss Red Cross (SRC), Zürich‐Schlieren, Switzerland;4. School of Medicine, The University of Queensland, Brisbane, Queensland, Australia;5. Department of Neurology, University and University Hospital Zürich, Zurich, Switzerland;6. Blood Transfusion Service Zürich, Swiss Red Cross (SRC), Zürich‐Schlieren, Switzerland
Abstract:
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号