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Essai de translocation héréditaire
Test de la translocation héréditaire
Test de la translocation transmissible
Translocation Robertsonienne
Translocation autosome X
Translocation d'X-autosomes
Translocation réciproque équilibrée x-autosome
Translocation x-autosome
Translocation équilibrée x-autosome

Translation of "Translocation x-autosome " (French → English) :

translocation x-autosome

x-autosome translocation
Amélioration génétique des animaux
Animal Breeding


translocation équilibrée x-autosome

balanced x-autosome translocation
Amélioration génétique des animaux
Animal Breeding


translocation réciproque équilibrée x-autosome

balanced reciprocal x-autosome translocation
Amélioration génétique des animaux
Animal Breeding


translocation autosome X

X-autosome translocation
IATE - Health
IATE - Health


translocation d'X-autosomes

X-autosome translocation
IATE - Health | Natural and applied sciences
IATE - Health | Natural and applied sciences


essai de translocation héréditaire | test de la translocation héréditaire | test de la translocation transmissible

heritable translocation test
IATE - Health
IATE - Health


carcinome rénal associé à une translocation de la famille MiT

A rare subtype of renal cell carcinoma with recurrent genetic abnormalities, harboring rearrangements of the TFE3 (Xp11 t-RCC) or TFEB [t(6; 11) t-RCC] genes. The t(6; 11) t-RCC has distinctive histologic features of biphasic appearance with larger epi
SNOMEDCT-BE (disorder) / 764694005
SNOMEDCT-BE (Xp11 t-RCC) or TFEB [t(6;11) t-RCC] genes. The t(6;11) t-RCC has distinctive histologic features of biphasic appearance with larger epi / 764694005


Trisomie 21, translocation

Trisomy 21, translocation
WORLD HEALTH ORGANIZATION ICD-10: Q90.2
WORLD HEALTH ORGANIZATION ICD-10: Q90.2


translocation Robertsonienne

Robertsonian translocation
SNOMEDCT-CA (anomalie morphologique) / 81568008
SNOMEDCT-CA (anomalie morphologique) / 81568008


ADCME - autosomal dominant cortical myoclonus and epilepsy

An inherited epileptic syndrome characterized by cortical hand tremors, myoclonic jerks and occasional generalized or focal seizures with a non-progressive or very slowly progressive disease course, and no signs of early dementia or cerebellar ataxia
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001




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Translocation x-autosome

Date index:2021-04-29 -

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