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ACV
Blood
CMT
Charcot-Marie-Tooth disease
Congenital afibrinogenaemia Deficiency AC globulin
Deficiency of factor I
Element of group VII
Fibrin-stabilizing
Fibrinogen
HMSN
HMSN III
HMSN VII
Hageman
Hereditary motor and sensory neuropathy
II
Labile
MPS VII
Morquio
Mucopolysaccharidosis type VII
PMA
Peroneal muscular atrophy
Proaccelerin
Prothrombin
Sanfilippo
Sly disease
Sly syndrome
Stable
Stuart-Prower
V
VII
X
XII
XIII

Vertaling van "hmsn vii " (Engels → Nederlands) :

HMSN VII
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
hereditaire motorische en sensorische neuropathie met retinitis pigmentosa
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
mucopolysaccharidosis type VII | Sly disease | Sly syndrome | MPS VII [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
beta-glucuronidase deficiëntie | mucopolysaccharidose VII | Sly syndroom
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Charcot-Marie-Tooth disease | hereditary motor and sensory neuropathy | peroneal muscular atrophy | CMT [Abbr.] | HMSN [Abbr.] | PMA [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
hereditaire motorische en sensorische neuropathie | ziekte van Charcot-Marie-Tooth | HMSN [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Blood (WBC) screen for MPS type VII
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
screenen op mucopolysacharidose VII in leukocyten in bloed
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
HMSN III
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
hereditaire motorische en sensorische neuropathie type 3
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
element of group VII
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
elementen uit groep VII
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
bèta-glucuronidasedeficiëntie | mucopolysaccharidose, type III, IV, VI, VII | syndroom (van) | Maroteaux-Lamy (licht)(ernstig) | syndroom (van) | Morquio(-achtig)(klassiek) | syndroom (van) | Sanfilippo (type B)(type C)(type D)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
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://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
Agreement on Implementation of Article VII of the General Agreement on Tariffs and Trade 1994 [ ACV ]
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
Overeenkomst inzake de toepassing van artikel VII van de Algemene Overeenkomst inzake Tarieven en Handel 1994 [ ACV | OTTH ]
https://www.termdat.bk.admin.c (...) (...) [HTML] [2018-01-01]
https://www.termdat.bk.admin.c (...) [HTML] [2018-01-01]


Anderen hebben gezocht naar : charcot-marie-tooth disease     congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     hmsn iii     hmsn vii     hageman     mps vii     morquio     sanfilippo     sly disease     sly syndrome     stuart-prower     element of group vii     fibrin-stabilizing     fibrinogen     hereditary motor and sensory neuropathy     labile     peroneal muscular atrophy     proaccelerin     prothrombin     stable     


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Date index: 2022-11-18
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