Open AccessChromosomal aberrations as the cause of a complex phenotype in children with primary immunodeficiencies
Author(s) -
Natalia Kuzmenko,
Anna Mukhinа,
Ю. А. Родина,
Elena Deripapa,
А. Л. Хорева,
О. А. Швец,
Ekaterina Deordieva,
V.I. Burlakov,
А. А. Роппельт,
Д. В. Юхачёва,
A.A. Moiseeva,
С. П. Хомякова,
М. Ю. Алексенко,
В. В. Захарова,
Е. В. Райкина,
Anna Shcherbina
Publication year - 2021
Publication title -
voprosy gematologii/onkologii i immunopatologii v pediatrii
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.108
H-Index - 3
eISSN - 2414-9314
pISSN - 1726-1708
DOI - 10.24287/1726-1708-2020-19-4suppl-62-67
Subject(s) - primary immunodeficiency , immunodeficiency , phenotype , severe combined immunodeficiency , x chromosome , chromosome , biology , medicine , immune system , gene , genetics