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...

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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927891/
https://www.ncbi.nlm.nih.gov/pubmed/32241844
http://dx.doi.org/10.3324/haematol.2019.242677

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927891/
https://www.ncbi.nlm.nih.gov/pubmed/32241844
http://dx.doi.org/10.3324/haematol.2019.242677

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