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immunology and genetics journal
سال:2019 - دوره:2 - شماره:4
autoimmunity in patients with hyper igm syndrome
- صفحه:196-206
first case of x-linked recessive anhidrotic ectodermal dysplasia with immunodeficiency from iran with unusual aspergillus infection
- صفحه:213-220
gastrointestinal manifestations in patients with common variable immunodeficiency
- صفحه:185-195
nfkb2 mutation in a patient with lymphopenia and extreme cold sensitivity (a case report)
- صفحه:207-212
precision medicine as treatment for primary immunodeficiency and immune dysregulation
- صفحه:153-172
why should trec and krec quantification assay be concerned to screen of newborns in developing countries?
- صفحه:173-184
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