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CEFR
Common European Framework of Reference for Languages
Disappearing language
Early foreign language acquisition
Early foreign language learning
Early language learning
Early second language acquisition
Early second language learning
Early stages foreign language learning
Early-stage foreign language acquisition
Early-stage foreign language learning
Endangered language
First language
Foreign language competence
Heritage language
L1
Language
Language competence
Language of origin
Language proficiency
Language qualifications
Language skills
MERU
Maharishi European Research University
Meru
Meru language
Minority language
Mother language
Mother tongue
Native language
Threatened language

Traduction de «Meru language » (Anglais → Français) :



language skills [ CEFR | Common European Framework of Reference for Languages | foreign language competence | language competence | language proficiency | language qualifications ]

compétence linguistique [ cadre européen commun de référence pour les langues | CECR | compétences en langues étrangères | compétences linguistiques | connaissances linguistiques ]




early foreign language acquisition | early foreign language learning | early language learning | early second language acquisition | early second language learning | early stages foreign language learning | early-stage foreign language acquisition | early-stage foreign language learning

apprentissage précoce d'une langue étrangère


Maharishi European Research University | MERU [Abbr.]

Université européenne de recherches Maharishi




minority language [ disappearing language | endangered language | threatened language ]

langue minoritaire [ langue en péril | langue en voie d'extinction | langue en voie de disparition | langue menacée ]


first language | heritage language | language of origin | mother language | mother tongue | native language | L1 [Abbr.]

langue d'origine | langue I | langue maternelle | langue première


A rare chromosomal anomaly syndrome resulting from a partial deletion of the long arm of chromosome 10. The disease has a highly variable phenotype with principle characteristics of developmental delay (usually of language and speech), variable cogni

monosomie non distale 10q


A rare epilepsy syndrome characterized by late-onset (after 1 year old) epileptic spasms that occur in clusters, associated with tonic seizures, atypical absences and cognitive deterioration. Language difficulties and behavior problems are frequently

spasme cryptogénique à début tardif


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