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Anomaly
Hereditary leukocytic hypersegmentation
Hyposegmentation
Leukomelanopathy
May-Hegglin
Nuclear anomaly
Pelger nuclear anomaly
Pelger-Huet anomaly
Pelger-Huët

Vertaling van "pelger nuclear anomaly " (Engels → Nederlands) :







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

anomalie (granulatie)(granulocyt) of syndroom van | Alder | anomalie (granulatie)(granulocyt) of syndroom van | May-Hegglin | anomalie (granulatie)(granulocyt) of syndroom van | Pelger-Huët | hereditaire | leukocytaire | hypersegmentatie | hereditaire | leukocytaire | hyposegmentatie | hereditaire | leukomelanopathie


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

progressieve externe oftalmoplegie, myopathie, emaciatie


Retinal dystrophy with inner nuclear layer and ganglion cell anomalies

retinale dystrofie met binnenste retinale disfunctie en ganglioncelanomalieën




Anderen hebben gezocht naar : anomaly or syndrome alder     may-hegglin     pelger nuclear anomaly     pelger-huet anomaly     pelger-huët     hyposegmentation     leukomelanopathy     nuclear anomaly     


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Date index: 2024-09-05
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