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21q-syndrome
Antimongolism
Contra-type of Down syndrome
DSAT
Down Syndrome Association of Metropolitan Toronto
Down Syndrome Association of Toronto
Down syndrome
Down's Syndrome Congress
Down's syndrome
G-deletion syndrome 1
Kalmuk idiocy
Langdon Down syndrome
Mongol
Mongolian
Mongolian idiocy
Mongolian imbecility
Mongolism
Mongoloid
Mongoloid idiocy
Mongoloid imbecility
Monosomy 21
Mothers of Children With Down Syndrome
Mothers of Young Mongoloids
NDSC
National Down Syndrome Congress
National Down's Syndrome Congress
PODSC
Parents of Down Syndrome Children
Person with Down syndrome
Person with trisomy 21
Trisomic
Trisomic 21
Trisomy 21
Trisomy 21 syndrome

Translation of "Langdon Down syndrome " (English → French) :

Down syndrome | Down's syndrome | trisomy 21 | Langdon Down syndrome | trisomy 21 syndrome | mongolism | mongoloid idiocy | mongolian idiocy | mongoloid imbecility | mongolian imbecility

trisomie 21 | syndrome de Down | maladie de Down | syndrome de Langdon Down | idiotie furfuracée | acromimie | mongolisme | idiotie mongoloïde | idiotie mongolienne | imbécillité mongolienne | imbécillité mongoloïde
médecine > sémiologie et pathologie | biologie > génétique
médecine > sémiologie et pathologie | biologie > génétique


National Down Syndrome Congress [ NDSC | National Down's Syndrome Congress | Down's Syndrome Congress ]

National Down Syndrome Congress [ NDSC | National Down's Syndrome Congress | Down's Syndrome Congress ]
Organizations, Administrative Units and Committees
Organismes, unités administratives et comités


A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c

leucémie aigüe myéloïde héréditaire
SNOMEDCT-BE (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c / 764940002
SNOMEDCT-BE (disorder) / 764940002


Parents of Down Syndrome Children [ PODSC | Mothers of Children With Down Syndrome | Mothers of Young Mongoloids ]

Parents of Down Syndrome Children [ PODSC | Mothers of Children With Down Syndrome | Mothers of Young Mongoloids ]
Organizations, Administrative Units and Committees
Organismes, unités administratives et comités


Down Syndrome Association of Toronto [ DSAT | Down Syndrome Association of Metropolitan Toronto ]

Down Syndrome Association of Toronto [ DSAT | Down Syndrome Association of Metropolitan Toronto ]
Regional and Municipal Gov. Bodies and Committees | Human Diseases - Various
Organismes et comités de gouv. régionaux ou municipaux | Maladies humaines diverses


Down syndrome | Down's syndrome | Kalmuk idiocy | Mongolian idiocy | Mongolism | Trisomy 21

maladie de Down | maladie de Langdon Down | mongolisme | syndrome de Down | trisomie | trisomie 21
IATE - Health
IATE - Health


antimongolism | contra-type of Down syndrome | G-deletion syndrome 1 | monosomy 21 | 21q-syndrome

anti-mongolisme | contretype du syndrome de Down | monosomie 21 | syndrome 21 q-
biologie > cytogénétique
biologie > cytogénétique


trisomic | person with Down syndrome | person with trisomy 21 | trisomic 21 | mongol | mongolian | mongoloid

trisomique | personne trisomique 21 | personne atteinte de trisomie 21 | personne atteinte du syndrome de Down | trisomique 21 | mongolien | mongoloïde
médecine > sémiologie et pathologie | biologie > génétique | appellation de personne
médecine > sémiologie et pathologie | biologie > génétique | appellation de personne


Down syndrome

syndrome de Down
SNOMEDCT-BE (disorder) / 41040004
SNOMEDCT-BE (disorder) / 41040004


A recently described syndrome with characteristics of Wolff-Parkinson-White syndrome, variable developmental delay and facial dysmorphism. Dysmorphic features include macrocephaly, hypertelorism, down-slanting palpebral fissures and microstomia. This

syndrome de microdélétion 20p12.3
SNOMEDCT-BE (disorder) / 719650004
SNOMEDCT-BE (disorder) / 719650004




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'Langdon Down syndrome'

Date index:2024-01-12 -

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