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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

Vertaling van "histocompatibility system " (Engels → Frans) :



histocompatibility system

système d'histocompatibilité




human leukocyte antigen complex [ HLA complex | HLA histocompatibility system | HLA system | human major histocompatibility complex ]

système majeur d'histocompatibilité pour les humains [ système HLA | système LY-li ]


Histocompatibility antigen type

type d'antigène d'histocompatibilité


Major histocompatibility complex class I deficiency

Déficit en complexe majeur d'histocompatibilité classe I


major histocompatibility complex | MHC

complexe majeur d'histocompatibilité | CMH


minor histocompatibility antigen

antigène mineur d'histocompatibilité


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

syndrome de retard de développement-ostéopénie-anomalies ectodermiques


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

syndrome de Neu-Laxova




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Date index: 2024-04-04
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