Congenital haemolytic anaemia resulting from glucose phosphate isomerase deficiency: genetics, clinical picture, and prenatal diagnosis.

Author:

Whitelaw A G,Rogers P A,Hopkinson D A,Gordon H,Emerson P M,Darley J H,Reid C,Crawfurd M A

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference32 articles.

1. Glucose phosphate isomerase deficiency: evidence for in vivo instability of an enzyme variant with hemolysis;Arnold, H.; Blume, K.G.; Engelhardt, R.; Lohr, G.W.;Blood,1973

2. Glucose phosphate isomerase deficiency type Liege-new variant with congenital nonspherocytic hemolytic anemia;Arnold, H.; Dodinal-Versie, J.; Lambotte, C.; Lohr, G.W.; Van Der Hofstedt, J.;Blut,1977

3. Hereditary hemolytic anemia associated with glucose phosphate isomerase (GPI) deficiency-a new enzyme defect of human erythrocytes;Baughan, M.A.; Valentine, W.N.; Paglia, D.E.; Ways, P.O.; Simons, E.R.; DeMarsh, Q.B.;Blood,1968

4. International committee for standardization in haematology: recommended methods for red-cell enzyme analysis;Beutler, E.; Blume, K.G.; Kaplan, J.C.; Lohr, G.W.; Ramot, B.; Valentine, W.N.;British Journal of Haematology,1977

5. Glucosephosphate-isomerase (GPI) deficiency: GPI Elyria;Beutler, E.; Sigalove, W.H.; Muir, W.A.; Matsumoto, F.; West, C.;Annals of Internal Medicine,1974

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