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Anomaly
False shift to the left
Hereditary leukocytic hypersegmentation
Hyposegmentation
Leukomelanopathy
May-Hegglin
Nuclear anomaly
Pelger nuclear anomaly
Pelger's anomaly
Pelger's nuclear anomaly
Pelger-Huët
Pelger-Huët anomaly
Pelger-Huët nuclear anomaly
Pelger-Huët phenomenon

Translation of "pelger nuclear anomaly " (English → French) :

Pelger nuclear anomaly

anomalie nucléaire familiale de Pelger-Huet
IATE - Health
IATE - Health


Pelger-Huët anomaly | Pelger's anomaly | Pelger's nuclear anomaly | Pelger-Huët nuclear anomaly | Pelger-Huët phenomenon | false shift to the left

anomalie de Pelger-Huët
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie
biologie > cytogénétique | biologie > embryologie | médecine > sémiologie et pathologie


nuclear anomaly

anomalie nucléaire
IATE - Health
IATE - Health


Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy

Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire
WORLD HEALTH ORGANIZATION ICD-10: D72.0
WORLD HEALTH ORGANIZATION ICD-10: D72.0


Retinal dystrophy with inner nuclear layer and ganglion cell anomalies

dystrophie rétinienne avec anomalies de la couche nucléaire interne et des cellules ganglionnaires
SNOMEDCT-BE (disorder) / 774152007
SNOMEDCT-BE (disorder) / 774152007


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterised by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'OEP-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009


A rare mitochondrial oxidative phosphorylation disorder due to nuclear deoxyribonucleic acid anomalies. The disease is characterized by progressive external ophthalmoplegia without diplopia, cerebellar atrophy, proximal skeletal muscle weakness with

syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation
SNOMEDCT-BE (disorder) / 764733009
SNOMEDCT-BE (disorder) / 764733009




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'pelger nuclear anomaly'

Date index:2021-07-05 -

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