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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Dextrinosis
Familia
Forbes glycogenosis
GSD IV
Gierke's disease
Glycogen disease
Glycogen storage disease
Glycogen storage disease I
Glycogen storage disease type IV
Glycogenopathy
Glycogenoses
Glycogenosis
Glycogenosis IV
Hepatorenal glycogenosis
Hers glycogenosis
Najjar-Andersen syndrome
PIG - Pulmonary interstitial glycogenosis
Type 1 glycogenosis
Type I glycogen storage disease
Von Gierke's disease

Traduction de «glycogenosis nos » (Anglais → Français) :



Hers glycogenosis

glycogénose de Hers | maladie glycogénique de Hers




type I glycogen storage disease [ von Gierke's disease | Gierke's disease | type 1 glycogenosis | glycogen storage disease I | hepatorenal glycogenosis ]

maladie de von Gierke [ glycogénose de type I | glycogénose hépato-rénale ]




Andersen's disease [ Andersen disease | Najjar-Andersen syndrome | glycogenosis IV | glycogen storage disease type IV | GSD IV | alpha 1,4-glucan-6-glucosyl transferase deficiency | amylopectinosis brancher deficiency | brancher enzyme deficiency | brancher deficiency | amylopectinosis | familia ]

maladie d'Andersen [ glycogénose musculaire type IV ]


glycogen storage disease [ glycogen disease | glycogenosis ]

glycogénose


glycogen storage disease | glycogenosis | glycogenopathy | dextrinosis | glycogenoses

glycogénose | thésaurose glycogénique | glycogénoses


PIG - Pulmonary interstitial glycogenosis

glycogénose interstitielle pulmonaire


A rare and isolated orofacial defect with manifestation of incomplete median clefts of both the lower lip (limited to the vermilion, with no muscle involvement) and upper lip (with muscle involvement), double labial frenulum and fusion of the upper g

fente labiale médiane supérieure et inférieure, forme familiale




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Date index: 2022-09-18
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