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American Journal of Medical Genetics
|
October 28, 1996
Plasma hyaluronidase activity in mucolipidoses II and III: marked differences from other lysosomal enzymes
M R Natowicz, Y Wang
American Journal of Medical Genetics
|
January 15, 1994
Genetic disorders that masquerade as multiple sclerosis
M R Natowicz, B Bejjani
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 9, 1996
Human serum hyaluronidase: characterization of a clinical assay
M R Natowicz, Y Wang
Current Opinion in Pediatrics
|
December 1, 1996
Heterozygote screening for Tay-Sachs disease: past successes and future challenges
M R Natowicz, E M Prence
Clinical Chemistry
|
April 1, 1992
Diagnosis of alpha-mannosidosis by measuring alpha-mannosidase in plasma
E M Prence, M R Natowicz
BMJ (Clinical Research Ed.)
|
September 19, 1992
The allure of genetic explanations
J S Alper, M R Natowicz
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 19, 2008
Late-onset Tay-Sachs disease presenting as a childhood stutter
B E Shapiro, M R Natowicz
American Journal of Medical Genetics
|
May 1, 1994
Abnormal bile acids in the Smith-Lemli-Opitz syndrome
M R Natowicz, J E Evans
Journal of Inherited Metabolic Disease
|
January 1, 1993
Unusual biochemical presentation of GM1 gangliosidosis: markedly elevated levels of multiple plasma lysosomal enzyme activities
E M Prence, M R Natowicz
BMJ (Clinical Research Ed.)
|
December 11, 1993
Genetic testing and insurance
J S Alper, M R Natowicz
Page
of 6
Search research articles
Search
Showing results (1-10 of 53) with videos related to
Sort By:
Page
of 6
American Journal of Medical Genetics
|
October 28, 1996
Plasma hyaluronidase activity in mucolipidoses II and III: marked differences from other lysosomal enzymes
M R Natowicz, Y Wang
American Journal of Medical Genetics
|
January 15, 1994
Genetic disorders that masquerade as multiple sclerosis
M R Natowicz, B Bejjani
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
February 9, 1996
Human serum hyaluronidase: characterization of a clinical assay
M R Natowicz, Y Wang
Current Opinion in Pediatrics
|
December 1, 1996
Heterozygote screening for Tay-Sachs disease: past successes and future challenges
M R Natowicz, E M Prence
Clinical Chemistry
|
April 1, 1992
Diagnosis of alpha-mannosidosis by measuring alpha-mannosidase in plasma
E M Prence, M R Natowicz
BMJ (Clinical Research Ed.)
|
September 19, 1992
The allure of genetic explanations
J S Alper, M R Natowicz
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 19, 2008
Late-onset Tay-Sachs disease presenting as a childhood stutter
B E Shapiro, M R Natowicz
American Journal of Medical Genetics
|
May 1, 1994
Abnormal bile acids in the Smith-Lemli-Opitz syndrome
M R Natowicz, J E Evans
Journal of Inherited Metabolic Disease
|
January 1, 1993
Unusual biochemical presentation of GM1 gangliosidosis: markedly elevated levels of multiple plasma lysosomal enzyme activities
E M Prence, M R Natowicz
BMJ (Clinical Research Ed.)
|
December 11, 1993
Genetic testing and insurance
J S Alper, M R Natowicz
Page
of 6