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AC globuline
Aarskog
Cockayne
Congenitale afibrinogenemie
De Lange
Deficiëntie van
Deficiëntie van factor
Dubowitz
Dysfibrinogenemie
Fibrinestabiliserend
Fibrinogeen
Hageman
Holt-Oram
Hypoproconvertinemie
I
II
Klippel-Trenaunay-Weber
LBWC
Labiel
Nagel-patella
Noonan
Prader-Willi
Proaccelerine
Protrombine
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Stabiel
Stuart-Prower
Syndroom
Syndroom
Syndroom van
Syndroom van Abderhalden-Fanconi
Syndroom van Debré-Fanconi
Syndroom van Debré-de Toni-Fanconi
Syndroom van Owren
TAR-syndroom
Test van Owren
Thrombotest van Owren
Trombocytopenie met ontbreken van radius
V
VATER-syndroom
VII
X
XII
XIII
Ziekte van Owren
Ziektebeeld

Vertaling van "Syndroom van Owren " (Nederlands → Engels) :

syndroom van Owren
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Owren syndrome
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
test van Owren | thrombotest van Owren
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
Owren's buffer
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
syndroom | ziektebeeld
http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]
syndrome
http://users.ugent.be/~rvdstic (...) (...) [HTML] [2018-01-01]
http://users.ugent.be/~rvdstic (...) [HTML] [2018-01-01]
syndroom van Abderhalden-Fanconi | syndroom van Debré-de Toni-Fanconi | syndroom van Debré-Fanconi
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
A.-F.syndrome | cystine storage disease
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
congenitale afibrinogenemie | deficiëntie van | AC globuline | deficiëntie van | proaccelerine | deficiëntie van factor | I [fibrinogeen] | deficiëntie van factor | II [protrombine] | deficiëntie van factor | V [labiel] | deficiëntie van factor | VII [stabiel] | deficiëntie van factor | X [Stuart-Prower] | deficiëntie van factor | XII [Hageman] | deficiëntie van factor | XIII [fibrinestabiliserend] | dysfibrinogenemie (congenitaal) | hypoproconvertinemie | ziekte van Owren
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Congenital afibrinogenaemia Deficiency:AC globulin | proaccelerin | Deficiency of factor:I [fibrinogen] | II [prothrombin] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [fibrin-stabilizing] | Dysfibrinogenaemia (congenital) Hypoproconvertinaemia Owren's disease
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
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
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
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
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER
https://terminologie.nictiz.nl (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
LBWC (limb body wall complex)-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Limb body wall complex
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
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
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
Pseudohypoparathyroidism type Ia
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : ac globuline     aarskog     cockayne     dubowitz     hageman     holt-oram     lbwc     noonan     prader-willi     rubinstein-taybi     russell-silver     seckel     smith-lemli-opitz     stuart-prower     tar-syndroom     vater-syndroom     congenitale afibrinogenemie     de lange     deficiëntie     deficiëntie van factor     dysfibrinogenemie     fibrinestabiliserend     fibrinogeen     hypoproconvertinemie     labiel     nagel-patella     proaccelerine     protrombine     sirenomelie     stabiel     syndroom     syndroom van abderhalden-fanconi     syndroom van debré-fanconi     syndroom van debré-de toni-fanconi     syndroom van owren     test van owren     thrombotest van owren     trombocytopenie met ontbreken van radius     ziekte van owren     ziektebeeld     Syndroom van Owren     


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Date index: 2023-04-14
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