Synapse - Cancer Genetics

Cancer Genetics

Published by: Elsevier Inc.

People

Aypar

Groups

Search Within

Results (3)

Clinical utility of mate pair sequencing to detect diagnostic and prognostic chromosomal rearrangements and copy number changes in patients with acute myeloid leukemia

Meeting Abstract

Baughn, L. B.; Smoley, S. A.; Aypar, U.; Pitel, B. A.; Vasmatzis, G.; Johnson, S. H.; Smadbeck, J. B.; Peterson, J. F.; Geiersbach, K. B.; Van Dyke, D. L.; more...
Cancer Genetics (2018)

Fulltext@MSK | Save

Circulating cell-free DNA for non-invasive cancer management

Journal Article

Stewart, C. M.; Tsui, D. W. Y.
Cancer Genetics (2018)

Fulltext@MSK | Save

Assessing copy number aberrations and copy-neutral loss-of-heterozygosity across the genome as best practice: An evidence-based review from the Cancer Genomics Consortium (CGC) working group for chronic lymphocytic leukemia

Journal Article

Chun, K.; Wenger, G. D.; Chaubey, A.; Dash, D. P.; Kanagal-Shamanna, R.; Kantarci, S.; Kolhe, R.; Van Dyke, D. L.; Wang, L.; Wolff, D. J.; more...
Cancer Genetics (2018)

Fulltext@MSK | Save

Cancer Genetics – authorized name for:

Name	ISSN / ISBN	Publisher
Cancer Genetics	22107762	2018
Cancer Genetics	22107762	Elsevier Inc.
Cancer Genetics	2210-7762	Elsevier Inc.
Cancer Genetics	22107770	Elsevier Inc.
Cancer Genetics	22107762	2022
Cancer Genetics	2210-7762	Elsevier Inc.
Cancer Genetics	22107770	Elsevier Inc.
Cancer Genetics	2210-7762	Elsevier Science, Inc.
Cancer Genetics	2210-7762	Elsevier Inc.
Cancer Genetics	22107762	Unknown
Cancer Genetics	2210-7762	Elsevier Science, Inc.
Cancer Genetics	2210-7762	Unknown
Cancer Genetics	978-1-4419-6033-7	Springer