Vertaling van "Thurston syndrome " (Engels → Frans) :

Thurston syndrome
syndrome oro-facio-digital type 5

Thurston's conjecture | Thurston's geometrization conjecture
conjecture de géométrisation | conjecture de Thurston

Thurston-Holland sign [ Thurston Holland's fragment | Thurston Holland's corner sign ]
signe de Thurston-Holland

Thurstone Attitude Scale [ Thurstone attitude scale | Thurstone scale ]
échelle de L.L. Thurstone [ échelle d'attitude de Thurstone | échelle de Thurstone | méthode des juges | échelle à intervalles apparemment égaux ]

Thurstone's Comparative Judgment Model [ Thurstone model | thurstone's law of comparative judgment ]
modèle de Thurstone [ loi du jugement comparatif de Thurstone ]

Sturge-Weber syndrome | Dimitri-disease | Kalischer's syndrome | Krabbe's II syndrome | Parkes Weber's syndrome | Sturge's syndrome | Sturge's disease | Sturge-Kalischer-Weber syndrome | Sturge-Weber disease | Sturge-Weber-Dimitri syndrome | Weber-Dimitri syndrome | angioma capillare et venosum calcificans | angiomatosis meningo-oculofacialis | congenital neuroectodermal dysplasia | cutaneocerebral angioma | encephalotrigeminal angiomatosis | encephalotrigeminal syndrome | neurocutaneous syndrome
syndrome de Sturge-Weber | angiomatose encéphalotrigéminée de Sturge-Weber-Krabbe | angiomatose méningo-oculo-faciale | angiomatose neuro-cutanée | angiomatose neuro-oculo-cutanée | maladie de Sturge-Weber-Krabbe | neuro-ectodermo-dysplasie congénitale | syndrome de Brushfield-Wyatt | syndrome neuro-cutané | syndrome de Parkes-Weber | syndrome de Sturge-Weber-Krabbe | syndrome de Weber-Dimitri

Bardet-Biedl syndrome | Biedl's syndrome | Biemond's syndrome | Laurence-Moon-Biedl syndrome | Moon-Bardet-Biedl syndrome
syndrome de Laurence-Biedl | syndrome de Laurence-Moon-Bardet

blue sclera syndrome | Eddowes-Spurway syndrome | Eddowes'syndrome | Lobstein's syndrome | Spurway's syndrome
syndrome d'Eddowes

A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib
syndrome de Mœbius

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