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Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita
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 media...
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主要な著者: | , , , , , , , , |
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フォーマット: | Artigo |
言語: | Inglês |
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American Society of Hematology
2007
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主題: | |
オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1975834/ https://ncbi.nlm.nih.gov/pubmed/17468339 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2007-02-075598 |
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