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Deletions of 9q21.3 including NTRK2 are associated with severe phenotype
Author(s) -
Hancarova Miroslava,
Puchmajerova Alena,
Drabova Jana,
Karaskova Eliska,
Vlckova Marketa,
Sedlacek Zdenek
Publication year - 2015
Publication title -
american journal of medical genetics part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.36797
Subject(s) - phenotype , function (biology) , clinical phenotype , table (database) , genetics , biology , world wide web , computational biology , information retrieval , gene , computer science , data mining