Open AccesseP406: Germline 16p13.1 microdeletion identified during routine hematologic testing
Author(s) -
Katarzyna Thompson,
Reid G. Meyer,
Erik C. Thorland,
Patricia T. Greipp,
Linda B. Baughn,
J.L. Peterson,
Xinjie Xu,
Rhett P. Ketterling,
Nicole L. Hoppman
Publication year - 2022
Publication title -
genetics in medicine
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 3.509
H-Index - 128
eISSN - 1530-0366
pISSN - 1098-3600
DOI - 10.1016/j.gim.2022.01.441
Subject(s) - fusion gene , germline , microdeletion syndrome , genetics , biology , fluorescence in situ hybridization , myeloid leukemia , medicine , chromosome , cancer research , gene
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