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Agglutination titer
Blood titer
HA titer
HA titre
HI titer
HI titre
Haemagglutination inhibition titer
Haemagglutination inhibition titre
Haemagglutination titer
Haemagglutination titre
Hemagglutination inhibition titer
Hemagglutination inhibition titre
Hemagglutination titer
Hemagglutination titre
Hemoagglutination titer
Hemoagglutination titre
Normality
Rock that has to bend
Rock that has to curl
Rock that has to curve
Rock that has to cut
Rock that has to swing
Stone that has to bend
Stone that has to curl
Stone that has to curve
Stone that has to cut
Stone that has to swing
Titer
Titer test

Traduction de «HA titer » (Anglais → Français) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous
hemagglutination titer [ haemagglutination titer | hemoagglutination titer | hemagglutination titre | haemagglutination titre | hemoagglutination titre | HA titer | HA titre ]

titre hémagglutinant [ titre HA | titre en HA ]








hemagglutination inhibition titer [ haemagglutination inhibition titer | hemagglutination inhibition titre | haemagglutination inhibition titre | HI titer | HI titre ]

titre de l'inhibition de l'hémagglutination [ titre IH | titre en IH ]


rock that has to bend [ stone that has to bend | rock that has to curl | stone that has to curl | rock that has to curve | stone that has to curve | rock that has to swing | stone that has to swing | rock that has to cut | stone that has to cut ]

pierre qui doit bifurquer [ pierre qui doit courber | pierre qui doit couper ]


This syndrome has characteristics of severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw

syndrome de petite taille-valvulopathie cardiaque-dysmorphie


This syndrome has characteristics of Hirschsprung disease and absence or hypoplasia of the nails and distal phalanges of the thumbs and great toes (type D brachydactyly). It has been described in four males from one family (two brothers and two mater

syndrome de maladie de Hirschsprung-brachydactylie type D


This syndrome has characteristics of the association of total alopecia (present at birth), mild intellectual deficit and hypergonadotropic hypogonadism. It has been described in two brothers born to non consanguineous parents of Caucasian origin. Ele

syndrome d'alopécie-déficience intellectuelle-hypogonadisme hypergonadotrope


TRADUCTIONS EN CONTEXTE
The response may be evaluated by counting specific plaque-forming cells (PFC) in the spleen or by determining the titer of SRBC- or KLH-specific IgM antibody in the serum by ELISA, at the peak of the response.

La réponse peut être évaluée par comptage des cellules formatrices de plaques (CFP) spécifiques dans la rate ou par titrage sérique des anticorps IgM spécifiques aux GRM ou à la KLH par ELISA, au moment du pic de réponse.






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