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Automatic set
Automatic telephone set
Blood cell counter
Blood cell counting system
Class of sets
Collection of sets
Counting chamber
Dial set
Dial telephone
Dial telephone set
Dialling set
Family of sets
Family of sets indexed by I
Globulimeter
Hemacytometer
Hemacytometer counting chamber
Hemacytometer cover glass
Hemacytometer set
Platelet counting chamber
Rotary dial telephone set
Set of sets
Set prop man
Set prop woman
Set property man
Set property person
Set property woman
Stage property person
System of sets

Vertaling van "hemacytometer set " (Engels → Frans) :



blood cell counter | blood cell counting system | globulimeter | hemacytometer

cellule hématimétrique | compte-globules | globulimètre | hématimètre | hémocytomètre


hemacytometer cover glass

lamelle octogonale pour hématimètre


counting chamber [ platelet counting chamber | hemacytometer counting chamber ]

hématimètre


A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are intellectual disability, growth and developmental delay, facial dysmorphism (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous

trisomie 9 en mosaïque


family of sets | system of sets | family of sets indexed by I | set of sets | collection of sets | class of sets

famille d'ensembles | famille d'ensembles indexée par l'ensemble I | famille de sous-ensembles


dial telephone set | dial telephone | automatic telephone set | dial set | automatic set | dialling set | rotary dial telephone set

appareil téléphonique automatique | téléphone automatique | appareil téléphonique à cadran | appareil à cadran | téléphone à cadran


set property person | set property man | set property woman | set prop man | set prop woman | stage property person

accessoiriste de plateau


An extremely rare autosomal recessive disorder with characteristics of bilateral facial palsy with masked facies, sensorineural hearing loss, dysmorphic features (midfacial retrusion, low-set ears) and strabismus.

syndrome de paralysie faciale congénitale héréditaire-surdité variable


A partial autosomal monosomy with characteristics of a variable combination of developmental delay, intellectual disability, ectodermal, genitourinary and minor cardiac anomalies and specific dysmorphic features (prominent forehead and low-set ears).

monosomie non distale 12q




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'hemacytometer set' ->

Date index: 2022-08-02
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