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CD4 T cell
CD4 T-lymphocyte
CD4 lymphocyte
CD4+
CD4+ T4 helper
CD4+ T4 lymphocyte
CD8 T lymphocyte
CD8 cell
CD8 lymphocyte
CD8+ T cell
CD8+ cell
Cytotoxic T cell
Cytotoxic T lymphocyte
Helper CD4 cell
Helper T lymphocyte
Helper T-cell
Helper cell
Helper lymphocyte
Helper-inducer T-cell
Inducer T-lymphocyte
Inducer cell
Lymphocytic
Lymphocytic predominance
Other predominantly sexually transmitted diseases
T-helper cell
T4 cell
T4 helper
T8 cell
T8 lymphocyte
TIL
Tumor infiltrating lymphocyte
Tumor-derived activated cell
Tumor-infiltrating lymphocyte
Tumour infiltrating lymphocyte
White blood cell-related

Vertaling van "lymphocytic predominance " (Engels → Nederlands) :

Lymphocytic predominance

Hodgkin-lymfoom, nodulair lymfocytenrijk


CD4 lymphocyte | CD4 T cell | CD4 T-lymphocyte | CD4+ T4 helper | CD4+ T4 lymphocyte | helper CD4 cell | helper cell | helper lymphocyte | helper T lymphocyte | helper T-cell | helper-inducer T-cell | inducer cell | inducer T-lymphocyte | T4 cell | T4 helper | T-helper cell | CD4+ [Abbr.]

CD4-/OKT4-/Leu3-positieve cel | helper T-cel | helpercel | T4 cel | T4-cel | T4-helpercel | T4-lymfocyten | T-helpercel


CD8 cell | CD8 lymphocyte | CD8 T lymphocyte | CD8+ cell | CD8+ T cell | cytotoxic T cell | cytotoxic T lymphocyte | T8 cell | T8 lymphocyte

cytotoxische T-cel


A rare genetic lissencephaly with cerebellar hypoplasia subtype with characteristics of classical lissencephaly with thickened cortical gray matter (with either no discernable gradient, a predominantly posterior gradient, or a predominantly anterior

lissencefalie gelijktijdig met congenitale cerebellaire hypoplasie type A


tumor infiltrating lymphocyte | tumor-derived activated cell | tumor-infiltrating lymphocyte | tumour infiltrating lymphocyte | TIL [Abbr.]

tumorinfiltrerende lymfocyt | TIL [Abbr.]


A rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de

autosomaal recessieve intermediaire ziekte van Charcot-Marie-Tooth type C


Cap polyposis (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ

cap polyposis


lymphocytic | white blood cell-related

lymfocytair | met betrekking tot witte bloedlichaampjes


Other predominantly sexually transmitted diseases

overige hoofdzakelijk seksueel overdraagbare aandoeningen


Infections with a predominantly sexual mode of transmission

infecties met hoofdzakelijk seksuele overdracht




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'lymphocytic predominance' ->

Date index: 2024-04-05
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