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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Detaylı Bibliyografya
Yayımlandı:Haematologica
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Fondazione Ferrata Storti 2020
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Article
Online Erişim: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
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