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5p-syndrome
B1 deletion syndrome
Cat cry syndrome
Chromosome 5 short arm deletion
Cri du chat syndrome
Crying cat syndrome
Deletion of short arm of chromosome 4
Deletion of short arm of chromosome 5
Lejeune syndrome
Short arm of the chromosome

Translation of "Deletion short arm chromosome 5 " (English → French) :

A rare chromosomal anomaly syndrome resulting from a partial interstitial deletion of the short arm of chromosome 9. The disease has characteristics of mild to moderate developmental delay, hand tremors, myoclonic jerks, attention deficit-hyperactivi

syndrome de microdélétion 9p13
SNOMEDCT-BE (disorder) / 764725008
SNOMEDCT-BE (disorder) / 764725008


5p-syndrome | chromosome 5 short arm deletion | cri du chat syndrome | Lejeune syndrome

maladie du cri du chat
IATE - Health
IATE - Health


Deletion of short arm of chromosome 4

Délétion du bras court du chromosome 4
WORLD HEALTH ORGANIZATION ICD-10: Q93.3
WORLD HEALTH ORGANIZATION ICD-10: Q93.3


Deletion of short arm of chromosome 5

Délétion du bras court du chromosome 5
WORLD HEALTH ORGANIZATION ICD-10: Q93.4
WORLD HEALTH ORGANIZATION ICD-10: Q93.4


cri du chat syndrome | cat cry syndrome | crying cat syndrome | deletion of short arm of chromosome 5 | B1 deletion syndrome

syndrome du cri du chat | syndrome plurimalformatif de Lejeune | maladie du cri du chat | syndrome de Lejeune
biologie > embryologie | médecine > sémiologie et pathologie
biologie > embryologie | médecine > sémiologie et pathologie


A rare chromosomal anomaly syndrome, resulting from a partial interstitial micro duplication of the short arm of chromosome 7. The disease has characteristics of intellectual disability, psychomotor and speech delay, craniofacial dysmorphism (includi

syndrome de microduplication 7p22.1
SNOMEDCT-BE (includi / 764703002
SNOMEDCT-BE (disorder) / 764703002


short arm of the chromosome

bras court du chromosome
biologie > cytogénétique
biologie > cytogénétique


A rare chromosomal anomaly syndrome resulting from a partial deletion of the long arm of chromosome 10. The disease has a highly variable phenotype with principle characteristics of developmental delay (usually of language and speech), variable cogni

monosomie non distale 10q
SNOMEDCT-BE (usually of language and speech), variable cogni / 770665005
SNOMEDCT-BE (disorder) / 770665005




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'Deletion short arm chromosome 5'

Date index:2021-03-18 -

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