Genetic heterogeneity in Gaucher disease.

Author:

Zlotogora J,Zaizov R,Klibansky C,Matoth Y,Bach G,Cohen T

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference27 articles.

1. Glucosylceramide lipidosis: Gaucher disease;Brady, R.O.; Barranger, J.A.,1983

2. Phenotypic manifestation of Gaucher disease: clinical features in 48 biochemically verified type I patients and comments on type II patients. In: Gaucher disease, a century of delineation and research;Kolodny, E.H.; Ullman, M.D.; Mankin, H.J.; Raghavan, S.S.; Topol, J.; Sullivan, J.L.,1982

3. Genetic heterogeneity in type I Gaucher disease. In: Gaucher disease, a century of delineation and research;Devine, E.A.; Beighton, P.; Petersen, E.M.; Desnick, R.J.,1982

4. Chronic Gaucher disease; heat resistance of leukocyte, B-glucocerebrosidase in relation to some clinical parameters;Klibansky, C.; Hoffman, J.; Zaizov, R.; Matoth, Y.; Pinchas, J.; DeVries, A.;Biomedicine,1973

5. A note on the development of Gaucher cells in a newborn infant;Bernstein, J.; Sheldon, W.E.;J Pediatr,1959

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