Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies-Reference-Cited by-同舟云学术

Clinical Utility of Targeted Next-Generation Sequencing Assay to Detect Copy Number Variants Associated with Myelodysplastic Syndrome in Myeloid Malignancies

Published:2021-04 Issue:4 Volume:23 Page:467-483
ISSN:1525-1578
Container-title:The Journal of Molecular Diagnostics
language:en
Short-container-title:The Journal of Molecular Diagnostics

Author:

Jiang Liqun,Pallavajjala Aparna,Huang Jialing,Haley Lisa^ORCID,Morsberger Laura,Stinnett Victoria^ORCID,Hardy Melanie,Park Rebecca,Ament Candice,Finch Alexandra,Shane Alison,Parish Rebecca,Nozari Azin,Long Patty^ORCID,Adams Emily^ORCID,Smith Kirstin,Parimi Vamsi,Dougaparsad Sam^ORCID,Long Lori,Gocke Christopher D.,Zou Ying S.^ORCID

Publisher

Elsevier BV

Subject

Molecular Medicine,Pathology and Forensic Medicine

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