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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: American Society of Hematology 2007
Matèries:
Clinical Trials and Observations
Accés en línia: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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