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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

Traduction de «pelger nuclear anomaly » (Anglais → Français) :

Pelger nuclear anomaly
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
anomalie nucléaire familiale de Pelger-Huet
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Pelger-Huët anomaly | Pelger's anomaly | Pelger's nuclear anomaly | Pelger-Huët nuclear anomaly | Pelger-Huët phenomenon | false shift to the left
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
anomalie de Pelger-Huët
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
nuclear anomaly
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
anomalie nucléaire
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Anomaly (granulation)(granulocyte) or syndrome:Alder | May-Hegglin | Pelger-Huët | Hereditary:leukocytic:hypersegmentation | hyposegmentation | leukomelanopathy
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anomalie (granulation) (granulocyte) ou syndrome de:Alder | May-Hegglin | Pelger-Huët | Hypersegmentation | Hyposegmentation | leucocytaire, héréditaire | Leucomélanopathie héréditaire
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Retinal dystrophy with inner nuclear layer and ganglion cell anomalies
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
dystrophie rétinienne avec anomalies de la couche nucléaire interne et des cellules ganglionnaires
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome d'OEP-myopathie-émaciation
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome d'ophtalmoplégie externe progressive-myopathie-émaciation
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


D'autres ont cherché : anomaly or syndrome alder     may-hegglin     pelger nuclear anomaly     pelger's anomaly     pelger's nuclear anomaly     pelger-huët     pelger-huët anomaly     pelger-huët nuclear anomaly     pelger-huët phenomenon     false shift to the left     hyposegmentation     leukomelanopathy     nuclear anomaly     


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Date index: 2024-02-07
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