家族性血小板疾病并急性髓系白血病倾向一例报告并文献复习

OBJECTIVE: To analyze the clinical features, bone marrow features, and gene mutations of children with familial platelet disorder with predisposition to myeloid leukemia（FPD/AML）caused by a RUNX1 germline mutation as well as their family members. METHODS: The clinical data and gene mutations of a ch...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2021
Materias:
论著
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120121/
https://www.ncbi.nlm.nih.gov/pubmed/33979975
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.007

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120121/
https://www.ncbi.nlm.nih.gov/pubmed/33979975
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2021.04.007

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