Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes

Increasing awareness about germline predisposition and the widespread application of unbiased whole exome sequencing contributed to the discovery of new clinical entities with high risk for the development of haematopoietic malignancies. The revised 2016 WHO classification introduced a novel categor...

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Detalles Bibliográficos
Autores principales: Sahoo, Sushree S., Kozyra, Emilia J., Wlodarski, Marcin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Ltd. 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388796/
https://www.ncbi.nlm.nih.gov/pubmed/33038986
http://dx.doi.org/10.1016/j.beha.2020.101197

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7388796/
https://www.ncbi.nlm.nih.gov/pubmed/33038986
http://dx.doi.org/10.1016/j.beha.2020.101197

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