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Journal of Medical Genetics
|
October 1, 1996
Heterozygosity for Tay-Sachs disease in non-Jewish Americans with ancestry from Ireland or Great Britain
M van Bael, M R Natowicz, J Tomczak, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 30, 1986
Sulfogalactocerebroside and bis-(monoacylglyceryl)-phosphate as activators of spleen glucocerebrosidase
E M Prence, K O Garrett, H Panitch, et al.
Acta Neuropathologica
|
January 1, 1992
Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studies
J Alroy, S H Schelling, J G Thalhammer, et al.
American Journal of Human Genetics
|
December 1, 1993
A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimation
Z Cao, M R Natowicz, M M Kaback, et al.
Human Mutation
|
January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies
B R Akerman, J Zielenski, B L Triggs-Raine, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
Journal of Medical Genetics
|
October 1, 1996
Heterozygosity for Tay-Sachs disease in non-Jewish Americans with ancestry from Ireland or Great Britain
M van Bael, M R Natowicz, J Tomczak, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
April 30, 1986
Sulfogalactocerebroside and bis-(monoacylglyceryl)-phosphate as activators of spleen glucocerebrosidase
E M Prence, K O Garrett, H Panitch, et al.
Acta Neuropathologica
|
January 1, 1992
Adult onset lysosomal storage disease in a Tibetan terrier: clinical, morphological and biochemical studies
J Alroy, S H Schelling, J G Thalhammer, et al.
American Journal of Human Genetics
|
December 1, 1993
A second mutation associated with apparent beta-hexosaminidase A pseudodeficiency: identification and frequency estimation
Z Cao, M R Natowicz, M M Kaback, et al.
Human Mutation
|
January 1, 1992
A mutation common in non-Jewish Tay-Sachs disease: frequency and RNA studies
B R Akerman, J Zielenski, B L Triggs-Raine, et al.
Page
of 3