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Adair Dighton syndrome
Blegvad-Haxthausen syndrome
Brittle bone disease
Brittle bone syndrome
Chlorosis tarda
Edwardsiella tarda
Familial porphyria cutanea tarda
Genus Edwardsiella
Glass bone disease
Late chlorosis
Lobstein disease
Lobstein’s disease
Osteogenesis imperfecta
Osteogenesis imperfecta tarda
Osteogenesis imperfecta type I
PCT
Porphyria cutanea tarda
Porphyria cutanea tarda type I
Porphyria cutanea tarda type II
Sporadic porphyria cutanea tarda

Traduction de «edwardsiella tarda » (Anglais → Français) :

Edwardsiella tarda, biogroup 1

Edwardsiella tarda, biogroupe 1




familial porphyria cutanea tarda | porphyria cutanea tarda | porphyria cutanea tarda type I | porphyria cutanea tarda type II | sporadic porphyria cutanea tarda | PCT [Abbr.]

porphyrie cutanée symptomatique | porphyrie cutanée tardive | porphyrie cutanée tardive de type I | porphyrie cutanée tardive de type II | porphyrie cutanée tardive familiale | porphyrie cutanée tardive sporadique | PCF [Abbr.] | PCS [Abbr.] | PCT [Abbr.]


osteogenesis imperfecta tarda

maladie de Lobstein [ ostéopsathyrose | maladie des sclérotiques bleues ]


porphyria cutanea tarda

porphyrie cutanée tardive | PCT | porphyrie cutanée symptomatique




Adair Dighton syndrome | Blegvad-Haxthausen syndrome | brittle bone disease | brittle bone syndrome | glass bone disease | Lobstein disease | Lobstein’s disease | osteogenesis imperfecta | osteogenesis imperfecta tarda | osteogenesis imperfecta type I

dysplasie périostale | maladie de Lobstein | maladie des os de verre | ostéogénèse imparfaite | ostéogenèse imparfaite tardive | ostéopsathyrose | syndrome d'Adair-Dighton | syndrome de Blegvad-Haxthausen






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