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Deletions of 9q21.3 including NTRK2 are associated with severe phenotype
Authors:Miroslava Hancarova  Alena Puchmajerova  Jana Drabova  Eliska Karaskova  Marketa Vlckova  Zdenek Sedlacek
Affiliation:Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic
Abstract:
Keywords:
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