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Amylopectinosis
Amylopectinosis brancher deficiency
Andersen disease
Andersen's disease
Brancher deficiency
Brancher enzyme deficiency
Dysostosis multiplex
Familia
GSD IV
Gargoylism
Glycogen storage disease type IV
Glycogenosis IV
Hurler syndrome
Hurler's disease
Hurler's syndrome
Hurler-Scheie syndrome
Lipochondrodystrophy
MPS I
MPS I S
MPS I-H
Morquio
Mucopolysaccharidosis I
Mucopolysaccharidosis type I
Mucopolysaccharidosis type I S
Mucopolysaccharidosis type I-H
Najjar-Andersen syndrome
Pfaundler-Hurler syndrome
Sanfilippo
Scheie syndrome
The Mucolipidosis Type IV Foundation of Canada
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Traduction de «Mucopolysaccharidosis type IV » (Anglais → Français) :

mucopolysaccharidosis type I | mucopolysaccharidosis type I S | Scheie syndrome | MPS I S [Abbr.]

maladie de Scheie | mucopolysaccharidose de type I | mucopolysaccharidose de type I S | MPS I-S [Abbr.]


Hurler-Scheie syndrome | mucopolysaccharidosis type I | mucopolysaccharidosis type I H/S | MPS I-H/S [Abbr.]

mucopolysaccharidose de type I | mucopolysaccharidose de type I H/S | syndrome de Hurler-Scheie | MPS I-H/S [Abbr.]


dysostosis multiplex | gargoylism | Hurler syndrome | Hurler's disease | Hurler's syndrome | lipochondrodystrophy | mucopolysaccharidosis I | mucopolysaccharidosis type I-H | Pfaundler-Hurler syndrome | MPS I [Abbr.] | MPS I-H [Abbr.]

dysostose multiple | gargoylisme | lipochondrodystrophie | maladie de Hurler | mucopolysaccharidose de type I | syndrome de Hurler | syndrome de Pfaundler-Hurler | MPS I [Abbr.] | MPS I-H [Abbr.]


Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)

Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)


Mucopolysaccharidosis, type I

Mucopolysaccharidose, type I


Mucopolysaccharidosis, type II

Mucopolysaccharidose, type II


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 ]


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The Mucolipidosis Type IV Foundation of Canada

La Fondation du Canada pour la Mucolipidosis Type IV


Telephone Secure Equipment (STU II) - Type IV Maintenance

Équipement de téléphonie discrète STU II type IV - Maintenance




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'Mucopolysaccharidosis type IV' ->

Date index: 2022-10-31
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