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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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書誌詳細
主要な著者: Alter, Blanche P., Baerlocher, Gabriela M., Savage, Sharon A., Chanock, Stephen J., Weksler, Babette B., Willner, Judith P., Peters, June A., Giri, Neelam, Lansdorp, Peter M.
フォーマット: Artigo
言語:Inglês
出版事項: American Society of Hematology 2007
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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