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CB
CB ham
CB user
CBS deficiency
CBS reference set
Citizen's band
Congenital afibrinogenaemia Deficiency AC globulin
Deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
G-6-p-d deficiency
G6PD deficiency
Glucose 6-dehydrogenase deficiency
Glucose-6-phosphate dehydrogenase deficiency
Haemolytic anaemia secondary to G6PD deficiency
Hageman
Hemolytic anemia secondary to G6PD deficiency
Hexokinase deficiency
II
Labile
PK
Proaccelerin
Prothrombin
Pyruvate kinase
Stable
Stuart-Prower
Triose-phosphate isomerase deficiency
V
VII
X
XII
XIII

Vertaling van "CBS deficiency " (Engels → Nederlands) :

CBS deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
deficiëntie van cystathionine-bètasynthase
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
G6PD-deficiëntie
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
haemolytic anaemia secondary to G6PD deficiency | haemolytic anaemia secondary to glucose-6-phosphate dehydrogenase deficiency | hemolytic anemia secondary to G6PD deficiency | hemolytic anemia secondary to glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
fosfaatdehydrogenase-deficiëntie | hemolytische anemie door G6PD-deficiëntie | hemolytische anemie door glucose-6
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
CB ham | CB user
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
CB-amateur | radio-amateur
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
CBS reference set
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
referentieset voor doodsoorzakenstatistiek
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
obesitas als gevolg van melanocortine-4-receptordeficiëntie
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://terminologie.nictiz.nl (...) [HTML] [2018-01-01]
CB | Citizen's band
http://www.franca.cfwb.be/t000 (...) (...) [HTML] [2018-01-01]
Citizens' band
http://www.franca.cfwb.be/t000 (...) (...) [HTML] [2018-01-01]
http://www.franca.cfwb.be/t000 (...) [HTML] [2018-01-01]
Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
anemie door vitamine B12-deficiëntie als gevolg van tekort aan 'intrinsic factor'
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]


Anderen hebben gezocht naar : cb ham     cb user     cbs deficiency     cbs reference set     citizen's band     congenital afibrinogenaemia deficiency ac globulin     deficiency of factor     g6pd deficiency     hageman     stuart-prower     deficiency     fibrin-stabilizing     fibrinogen     g-6-p-d deficiency     glucose 6-dehydrogenase deficiency     glucose-6-phosphate dehydrogenase deficiency     hexokinase deficiency     labile     proaccelerin     prothrombin     pyruvate kinase     stable     triose-phosphate isomerase deficiency     CBS deficiency     


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Date index: 2024-05-15
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