Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development

Hereditary predisposition syndromes to myeloid neoplasms: diseases, genes and mechanisms of development

With the development of modern next generation sequencing based DNA diagnostic methods, it has become possible to study hereditary predisposition to oncohematological diseases. Germline variants (mutations) of RUNX1, CEBPA, GATA2, ANKRD26, DDX41, FANC- (Fanconi anemia), etc. genes, associated with t...

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Main Authors: M. V. Makarova, M. V. Nemtsova, D. A. Chekini, D. K. Chernevskiy, O. V. Sagaydak, E. V. Kosova, A. A. Krinitsyna, M. S. Belenikin, P. A. Zeynalova
Format: Article
Language:Russian
Published: ABV-press 2024-04-01
Series:Онкогематология
Subjects:
hereditary cancer syndromes
hematological malignancies
next generation sequencing
Online Access:https://oncohematology.abvpress.ru/ongm/article/view/918
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