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Aarskog
Cockayne
De Lange
Dubowitz
Dérangementvan temporomandibulair gewricht
Holt-Oram
Klippel-Trenaunay-Weber
Knappende kaak
LBWC
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Costen
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
TAR-syndroom
Temporomandibulair syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziektebeeld

Vertaling van "syndroom van costen " (Nederlands → Engels) :

syndroom van Costen | temporomandibulair syndroom

Costen's syndrome | temporomandibular syndrome




dérangementvan temporomandibulair gewricht | pijn-disfunctiesyndroomvan temporomandibulair gewricht | knappende kaak | syndroom van Costen

Costen's complex or syndrome Derangement of temporomandibular joint Snapping jaw Temporomandibular joint-pain-dysfunction syndrome




syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi

A.-F.syndrome | cystine storage disease


syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER


LBWC (limb body wall complex)-syndroom

Limb body wall complex


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

Pseudohypoparathyroidism type Ia




datacenter (28): www.wordscope.be (v4.0.br)

'syndroom van costen' ->

Date index: 2023-03-09
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