Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors is a research paper published in The Application of Clinical Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 3 times.
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NIGMS NIH HHS
Grant: U54 GM104941
National Institutes of Health
Grant: 4U54GM104941-04
Delaware - CTR
FWCI
0.20
Citation Percentile
0.5%
Citation Trend
Fields of Study
Keywords
Sustainable Development Goals