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Article

Beyond HLA: the significance of genomic variation for allogeneic hematopoietic stem cell transplantation.

Blood - 15 Feb 2007

Mullally Ann, Ritz Jerome

Abstract excerpt

The last 2 years have seen much excitement in the field of genetics with the identification of a formerly unappreciated level of "structural variation" within the normal human genome. Genetic structural variants include deletions, duplications, and inversions in addition to the recently discovered, copy number variants. Single nucleotide polymorphisms are the most extensively evaluated variant within the genome...

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Share to Genetic Predisposition to Disease
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17008540
DOI: 10.1182/blood-2006-06-030858

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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