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Wiskott–Aldrich syndrome: review and report of a large family

Wiskott–Aldrich syndrome is a sex-linked recessive antibody-deficiency syndrome characterized by thrombocytopenia, eczema and increased susceptibility to infection. All forms of therapy are notably unsuccessful and these patients succumb in the first decade. Three cases of this syndrome are presente...

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Bibliografski detalji
Glavni autori: Stiehm, E. R., McIntosh, R. M.
Format: Artigo
Jezik:Inglês
Izdano: 1967
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1578833/
https://ncbi.nlm.nih.gov/pubmed/4166240
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