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H-2 histocompatibility system
H2
HLA complex
HLA histocompatibility system
HLA system
Histocompatibility antigen type
Histocompatibility system
Human leukocyte antigen complex
Human major histocompatibility complex
MHC
Major histocompatibility complex
Major histocompatibility complex class I deficiency
Minor histocompatibility antigen

Translation of "histocompatibility system " (English → French) :

H-2 histocompatibility system
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
système H-2
Immunology
Immunologie
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
histocompatibility system
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
système d'histocompatibilité
Immunology
Immunologie
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
H-2 histocompatibility system | H2
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
système H-2 | H2
médecine > allergologie | biologie > immunologie
médecine > allergologie | biologie > immunologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
human leukocyte antigen complex [ HLA complex | HLA histocompatibility system | HLA system | human major histocompatibility complex ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
système majeur d'histocompatibilité pour les humains [ système HLA | système LY-li ]
Immunology
Immunologie
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Histocompatibility antigen type
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
type d'antigène d'histocompatibilité
SNOMEDCT-CA (valeur de l'attribut) / 264835004
SNOMEDCT-CA (valeur de l'attribut) / 264835004
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Major histocompatibility complex class I deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Déficit en complexe majeur d'histocompatibilité classe I
WORLD HEALTH ORGANIZATION ICD-10: D81.6
WORLD HEALTH ORGANIZATION ICD-10: D81.6
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
major histocompatibility complex | MHC
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
complexe majeur d'histocompatibilité | CMH
biologie > génétique | biologie > biologie cellulaire
biologie > génétique | biologie > biologie cellulaire
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
minor histocompatibility antigen
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
antigène mineur d'histocompatibilité
médecine > allergologie | biologie > immunologie
médecine > allergologie | biologie > immunologie
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
This syndrome is characterized by the association of global developmental delay, osteopenia and skin anomalies. To date, only three cases (two brothers and one unrelated girl) have been reported. Central nervous system anomalies manifest as poor lang
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de retard de développement-ostéopénie-anomalies ectodermiques
SNOMEDCT-BE (two brothers and one unrelated girl) have been reported. Central nervous system anomalies manifest as poor lang / 717813005
SNOMEDCT-BE (disorder) / 717813005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Others have searched : h-2 histocompatibility system    hla complex    hla histocompatibility system    hla system    histocompatibility antigen type    histocompatibility system    human leukocyte antigen complex    human major histocompatibility complex    major histocompatibility complex    minor histocompatibility antigen    


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'histocompatibility system'

Date index:2022-04-21 -

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