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Carnation clover
Clover leaf interchange
Clover leaf intersection
Clover-leaf interchange
Clover-leaf intersection
Competent in French
Crimson clover
Department of French Guiana
French
French Guiana
French Overseas Department
French Overseas Territories
French clover
French honeysuckle
French overseas collectivity
French overseas department and region
Italian clover
Overseas territories of the French Republic
Spanish esparcet
Sulla
Sulla clover
Sulla sweetvetch
Territorial collectivities of the French Republic

Traduction de «french clover » (Anglais → Néerlandais) :

carnation clover | crimson clover | French clover | Italian clover

incarnaatklaver | inkarnaatklaver


French honeysuckle | Spanish esparcet | sulla | sulla clover | sulla sweetvetch

esparcette | rode hanekop


clover leaf interchange | clover leaf intersection | clover-leaf interchange | clover-leaf intersection

klaverblad | klaverbladkruising


French overseas collectivity [ French Overseas Territories | overseas territories of the French Republic | territorial collectivities of the French Republic ]

overzeese gemeenschap van Frankrijk [ Frankrijk LGO | LGO Frankrijk | overzeese gebieden van de Franse Republiek | territoriale gemeenschappen van de Franse Republiek ]


ability to comprehend spoken and written French and to speak and write in French | competent in French | French

Frans


French overseas department and region [ French Overseas Department ]

Overzees(e) departement en regio van Frankrijk [ Frankrijk Département d'Outre-Mer | Frankrijk DOM ]


French Guiana [ Department of French Guiana ]

Frans-Guyana


Syndrome with characteristics of short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies (including hypoplastic thumbs) and clubfoot. It has been described in 14 Brazilian families and in one unrelated French patient. Prominent lo

syndroom van kleine gestalte, Pierre Robin-sequentie, gespleten onderkaak, misvormingen van hand en klompvoet


Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The

spinocerebellaire ataxie type 11


Disease with characteristics of papulosquamous, ichthyosiform plaques on the limbs appearing shortly after birth and later manifestations including progressive ataxia, dysarthria, nystagmus and decreased reflexes. Reported in 25 members of one French

spinocerebellaire ataxie type 34




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Date index: 2024-06-25
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