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American elm
American white elm
Competent in French
Department of French Guiana
Elm pollen
European elm bark beetle
French
French Guiana
French Overseas Department
French Overseas Territories
French elm
French overseas collectivity
French overseas department and region
Lesser european elm bark beetle
Overseas territories of the French Republic
Small elm bark beetle
Small-leaved leaved elm
Smaller european elm bark beetle
Smooth-leaved elm
Soft elm
Territorial collectivities of the French Republic
White elm

Vertaling van "french elm " (Engels → Nederlands) :

French elm | small-leaved leaved elm | smooth-leaved elm

gladde iep | veldiep


European elm bark beetle | lesser european elm bark beetle | small elm bark beetle | smaller european elm bark beetle

kleine iepespintkever


American elm | American white elm | soft elm | white elm

Amerikaanse iep | Amerikaanse witte iep


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






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Date index: 2024-07-08
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