Gaucher's disease in South Africa.

Author:

Goldblatt J,Beighton P

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Spongy degeneration in the central nervous system in infancy;Barker, B.Q.; Robertson, J.T.; Victor, M.;Neurology,1964

2. A genetical analysis of thirty families with Wilson's disease;Bearn, A.G.;Annals ofHuman Genetics,1960

3. Gaucher's disease in Southern Africa;Beighton, P.; Sacks, S.;South African Medical Journal,1974

4. The diagnosis of the adult type of Gaucher's disease and its carrier state by demonstration of deficiency of B-glucosidase activity in perhipheral blood leucocytes;Beutler, E.; Kuhl, W.;Journal of Laboratory and Clinical Medicine,1970

5. Gaucher's disease-chronic adult type;Fried, K.; Matoth, Y.; Goldschmidt, E.,1963

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2. Challenges in the diagnosis and management of gaucher's disease in a young adult libyan arab female;Ibnosina Journal of Medicine and Biomedical Sciences;2021

3. The molecular characterization of Gaucher disease in South Africa;Clinical Genetics;2008-06-28

4. Interpreting Genetic Variability: The Effects of Shared Evolutionary History;Ciba Foundation Symposium 197 - Variation in the Human Genome;2007-09-28

5. Osteochondrodysplasias in South Africa;American Journal of Medical Genetics;1996-05-03

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