Work

Detection of Mutations in Inherited Bone Marrow Failure and Myelodysplastic Syndrome Genes Using Genomic Capture and Massively Parallel Sequencing in Clinical Diagnostics

Year: 2016

Type: article

Study design: Observational Study

Source: Blood

DOI: 10.1182/blood.v128.22.1507.1507

Authors: Siobán B. Keel, Tom Walsh, Colin Pritchard, Akiko Shimamura, Mary-Claire King, David Wu

Institutions: University of Washington, Boston Children's Hospital, Harvard University, Dana-Farber Cancer Institute

Language: English

Topic: Genomics and Rare Diseases

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2979495964

FWCI:

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