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'triple'-artrodese van enkel volgens Dunn
Aarskog
Benedikt
Claude
Cockayne
De Lange
Doorgedrukte triple fels
Dubowitz
Foville
Gejoggelde triple fels
Holt-Oram
Klippel-Trenaunay-Weber
Liggende triple fels
Millard-Gubler
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
TAR-syndroom
Triple-X-syndroom
Triple-negatief maligne neoplasma van mamma
Trisomie X
Trombocytopenie met ontbreken van radius
VATER-syndroom
Wallenberg
Weber

Traduction de «Triple-X-syndroom » (Néerlandais → Anglais) :

triple-X-syndroom | Trisomie X

47,XXX | karyotype 47, XXX | triple X syndrome | triplo X syndrome | trisomy X | XXX syndrome


doorgedrukte triple fels | gejoggelde triple fels | liggende triple fels

double lock cross welt


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


triple-negatief maligne neoplasma van mamma

The absence of staining for oestrogen receptor, progesterone receptor, and hormone epidermal growth factor receptor 2 (HER2/neu).


'triple'-artrodese van enkel volgens Dunn

Dunn operation


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

Pseudohypoparathyroidism type Ia




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Date index: 2024-06-07
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