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Aarskog
Benedikt
Bronsdiabetes
Claude
Cockayne
De Lange
Dubowitz
Foville
Haematochromatosis
Haemochromatosis
Hemochromatose
Holt-Oram
Klippel-Trenaunay-Weber
LBWC
Millard-Gubler
Nagel-patella
Noonan
Pigmentcirrose
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Bernard
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Hanot-Chauffard
Syndroom van Horner
Syndroom van Horner-Bernard
Syndroom van Troisier
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Wallenberg
Weber
Ziekte van Recklinghausen-Applebaum
Ziektebeeld

Traduction de «Syndroom van Troisier » (Néerlandais → Anglais) :

bronsdiabetes | haematochromatosis | haemochromatosis | hemochromatose | pigmentcirrose | syndroom van Hanot-Chauffard | syndroom van Troisier | ziekte van Recklinghausen-Applebaum

bronze diabetes | congenital pigmentary cirrhosis | haemochromatosis | hemochromatosis




syndroom van Bernard | syndroom van Horner | syndroom van Horner-Bernard

Bernard-Horner 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


syndroom (van) | Benedikt | syndroom (van) | Claude | syndroom (van) | Foville | syndroom (van) | Millard-Gubler | syndroom (van) | Wallenberg | syndroom (van) | Weber

Syndrome:Benedikt | Claude | Foville | Millard-Gubler | Wallenberg | Weber


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




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Date index: 2021-12-10
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