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Cerebral chromomycosis
Chromoblastomycosis
Chromomycosis
Chromomycosis and phaeomycotic abscess
Cutaneous chromomycosis
ESA
European accounting system
European system of accounts
European system of integrated economic accounts
European system of national and regional accounts
Hot igneous system
Igneous related geothermal system
Igneous related system
Magma system
Magmatic system
Partitioned multiprocessor system
Sectionalised multiprocessor system
Sectionalized multiprocessor system
Sectorised multiprocessor system
Sectorized multiprocessor system
Segmented multiprocessor system
Segmented system
Systemic chromomycosis

Vertaling van "systemic chromomycosis " (Engels → Nederlands) :



chromoblastomycosis | chromomycosis

chromoblastomycose | chromoblastomycosis | chromomycose | dermatitis verrucosa


Chromomycosis and phaeomycotic abscess

chromoblastomycose en feomycotisch abces






partitioned multiprocessor system | sectionalised multiprocessor system | sectionalized multiprocessor system | sectorised multiprocessor system | sectorized multiprocessor system | segmented multiprocessor system | segmented system

gepartitioneerd multiprocessorsysteem


European accounting system [ ESA | European system of accounts | European system of integrated economic accounts | European system of national and regional accounts | European system of national and regional accounts in the European Union ]

Europees stelsel van rekeningen [ ESR | Europees rekeningenstelsel | Europees stelsel van economische rekeningen | Europees systeem van nationale en regionale rekeningen | Europees systeem van rekeningen ]


hot igneous system | igneous related geothermal system | igneous related system | magma system | magmatic system

magmatisch systeem


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

syndroom van Neu-Laxova


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

algemene ontwikkelingsachterstand, osteopenie, ectodermaal defect-syndroom


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