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1 MP Coy
1st Military Police Company
2 MP Coy
2 Military Police Company
3 MP Coy Grn
3 Military Police Company Garrison
Dysostosis multiplex
Gargoylism
Hurler syndrome
Hurler's disease
Hurler's syndrome
Lipochondrodystrophy
MP HQ coy
MP rfl coy
MP ter coy
MPS I
MPS I-H
Military police headquarters company
Military police rifle company
Military police territorial company
Mucopolysaccharidosis I
Mucopolysaccharidosis type I-H
Pfaundler-Hurler syndrome

Translation of "mp coy " (English → French) :

1st Military Police Company [ 1 MP Coy ]

1re Compagnie de police militaire [ 1 Cie PM ]
Units (Regular Force, Armed Forces)
Unités (régulières, Forces armées)


3 Military Police Company Garrison [ 3 MP Coy Grn ]

3e Compagnie de police militaire de la garnison [ 3 Cie PM Grn ]
Units (Regular Force, Armed Forces)
Unités (régulières, Forces armées)


2 Military Police Company [ 2 MP Coy ]

2e Compagnie de police militaire [ 2 Cie PM ]
Units (Regular Force, Armed Forces)
Unités (régulières, Forces armées)


military police territorial company [ MP ter coy ]

compagnie territoriale de police militaire [ cp ter PM ]
Defence & warfare
Corps et services administratifs (Défense des états)


military police headquarters company [ MP HQ coy ]

compagnie d'état-major de police militaire [ cp EM PM ]
Defence & warfare
Corps et services administratifs (Défense des états)


military police rifle company [ MP rfl coy ]

compagnie de grenadiers de police militaire [ cp gren PM ]
Defence & warfare
Corps et services administratifs (Défense des états)


A group of tyrosine related oculocutaneous albinism (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i

albinisme oculo-cutané type 1
SNOMEDCT-BE (OCA1) that includes OCA1A, OCA1B, type 1 minimal pigment oculocutaneous albinism (OCA1-MP) and type 1 temperature sensitive oculocutaneous albinism (OCA1-TS). The phenotypic spectrum seen in OCA1 i / 765146000
SNOMEDCT-BE (disorder) / 765146000


Light/Medium Armoured Company | Light/Med Arm Coy [Abbr.]

compagnie blindée légère ou moyenne
IATE - European construction
IATE - European construction


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.]
IATE - Health
IATE - Health


Mucopolysaccharidosis, MPS-I

mucopolysaccharidose type 1
SNOMEDCT-BE (disorder) / 75610003
SNOMEDCT-BE (disorder) / 75610003




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'mp coy'

Date index:2023-11-29 -

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