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Bruton
Bruton's X-linked agammaglobulinemia
Bruton's disease
Bruton's hypogammaglobulinemia
Bruton's type agammaglobulinemia
Bruton's tyrosine kinase inhibitor
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
X-linked agammaglobulinaemia
XLA

Traduction de «Bruton's hypogammaglobulinemia » (Anglais → Néerlandais) :

Bruton's disease | Bruton's hypogammaglobulinemia | Bruton's X-linked agammaglobulinemia | X-linked agammaglobulinaemia | XLA [Abbr.]

Bruton hypogamma globulinemie | ziekte van Bruton


congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia

congenitale hypogammaglobulinemie


Bruton's type agammaglobulinemia

X-gebonden agammaglobulinemie


Bruton's tyrosine kinase inhibitor

aspecifieke proteïnetyrosinekinaseremmer


Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)

autosomale recessieve-agammaglobulinemie (Swiss type) | X-gebonden agammaglobulinemie [Bruton] (met groeihormoondeficiëntie)


Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding

hepatische veno-occlusieve ziekte, immuundeficiëntie




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Bruton's hypogammaglobulinemia ->

Date index: 2024-03-13
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