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Article

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita

27 Apr 2007

Abstract excerpt

Dyskeratosis congenita (DC) is an inherited bone marrow failure syndrome in which the known susceptibility genes (DKC1, TERC, and TERT) belong to the telomere maintenance pathway; patients with DC have very short telomeres. We used multicolor flow fluorescence in situ hybridization analysis of median telomere length in total blood leukocytes, granulocytes, lymphocytes, and several lymphocyte subsets to confirm...

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Share to Advanced biosensing and bioanalysis techniques
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Identifiers

PMID: 17468339
DOI: 10.1182/blood-2007-02-075598

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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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