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Anatomy of the auditory and vestibular system
Auditory anatomy
Auditory clocks
Auditory deficiency
Auditory disorder
Deficiency
G-6-p-d deficiency
G6PD deficiency
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Hexokinase deficiency
Human ear
Human ears
Mobility deficiency
Mobility difficulty
Mobility disability
Mobility impairment
PK
Pyruvate kinase
Reduction of auditory deficiency
Time-display methods
Triose-phosphate isomerase deficiency
Types of time-display methods
Typology of time-display methods

Vertaling van "auditory deficiency " (Engels → Nederlands) :



reduction of auditory deficiency

vermindering van de gehoorstoornis


G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

G6PD-deficiëntie


anatomy of the auditory and vestibular system | auditory anatomy | human ear | human ears

menselijk oor


Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child

obesitas als gevolg van melanocortine-4-receptordeficiëntie


Syndrome with characteristics of moderate to profound hearing loss in both ears and severe nearsightedness (high myopia). The hearing loss may be described as sensorineural or it may be caused by auditory neuropathy. The hearing loss is either presen

syndroom van perceptief gehoorverlies en hoge myopie


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase


auditory clocks | types of time-display methods | time-display methods | typology of time-display methods

tijdweergavemethodes


CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

3-methylglutaconzuuracidurie type 7


mobility deficiency | mobility difficulty | mobility disability | mobility impairment

beperkte mobiliteit | mobiele beperking




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Date index: 2023-11-27
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