Diagnosis and prognosis are supported by integrated assessment of next-generation sequencing in chronic myeloid malignancies. A real-life study

Next-generation sequencing (NGS) is used to investigate the presence of somatic mutations. The utility of incorporating routine sequencing to guide diagnosis and therapeutic decisions remains unclear. We report the findings of an observational, multicenter study that aimed to assess the impact of so...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Haematologica
Main Authors: Vantyghem, Sophie, Peterlin, Pierre, Thépot, Sylvain, Ménard, Audrey, Dubruille, Viviane, Debord, Camille, Guillaume, Thierry, Garnier, Alice, Le Bourgeois, Amandine, Wuilleme, Soraya, Godon, Catherine, Theisen, Olivier, Eveillard, Marion, Delaunay, Jacques, Maisonneuve, Hervé, Morineau, Nadine, Villemagne, Bruno, Vigouroux, Stéphane, Subiger, François, Lestang, Elsa, Loirat, Marion, Parcelier, Anne, Godmer, Pascal, Mercier, Mélanie, Trebouet, Adrien, Paz, Damien Luque, Le Calloch, Ronan, Le Clech, Lenaig, Bossard, Céline, Moreau, Anne, Ugo, Valérie, Hunault, Mathilde, Moreau, Philippe, Le Gouill, Steven, Chevallier, Patrice, Béné, Marie C., Le Bris, Yannick
Formato: Artigo
Idioma:Inglês
Publicado em: Fondazione Ferrata Storti 2020
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7927891/
https://ncbi.nlm.nih.gov/pubmed/32241844
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2019.242677
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados