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Journal of Inherited Metabolic Disease|March 1, 1997
Mutation prevalence among 47 unrelated Japanese patients with Gaucher disease: identification of four novel mutationsH Ida, O M Rennert, H Kawame, et al.
Brain & Development|November 1, 1994
Pathological and biochemical studies of fetal Krabbe diseaseH Ida, O M Rennert, K Watabe, et al.
Blood Cells, Molecules & Diseases|June 6, 1998
Type 1 Gaucher disease: phenotypic expression and natural history in Japanese patientsH Ida, O M Rennert, T Ito, et al.
Acta Paediatrica Japonica : Overseas Edition|June 1, 1996
Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1H Ida, O M Rennert, T Ito, et al.
Human Genetics|September 10, 1999
Clinical and genetic studies of Japanese homozygotes for the Gaucher disease L444P mutationH Ida, O M Rennert, K Iwasawa, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 24, 1999
Psychiatric inpatients and chromosome deletions within 22q11.2S Sugama, T Namihira, R Matsuoka, et al.
Clinical Nephrology|April 5, 2000
Focal segmental glomerulosclerosis in a patient with Prader-Willi syndromeH Mochizuki, K Joh, N Matsuyama, et al.
Human Reproduction (Oxford, England)|September 1, 1993
Presence and possible function of activin-like substance in human follicular fluidM Sadatsuki, O Tsutsumi, R Sakai, et al.
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