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Autosomaal dominante limb-girdle-spierdystrofie type 1B
Central-core-disease
Congenitale spierdystrofie
Congenitale spierdystrofie type 1B
Fibre-type disproportion
Minicore disease
Multicore disease
Myopathie
Myotubulair
NNO
Nemaline lichaampjes

Vertaling van "Congenitale spierdystrofie type 1B " (Nederlands → Engels) :

congenitale spierdystrofie type 1B

Congenital muscular dystrophy type 1B (disorder)


central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes

Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline


autosomaal dominante limb-girdle-spierdystrofie type 1B

Autosomal dominant limb girdle muscular dystrophy type 1B


autosomaal dominante 'limb-girdle'-spierdystrofie type 1B

Autosomal dominant limb girdle muscular dystrophy type 1B




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'Congenitale spierdystrofie type 1B' ->

Date index: 2024-01-03
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