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Canadian Journal of Biochemistry
|
June 1, 1979
Binding of mitochondrial malate dehydrogenase to mitoplasts
P M Strasberg, K A Webster, H V Patel, et al.
Biochemical Genetics
|
August 1, 1979
Mitochondrial malic enzyme in mosaic skeletal muscle of mouse chimeras
P M Frair, P M Strasberg, K B Freeman, et al.
American Journal of Human Genetics
|
August 1, 1991
Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl
J T Clarke, W L Greer, P M Strasberg, et al.
The Journal of Clinical Psychiatry
|
August 1, 1995
Late-onset Tay-Sachs disease presenting as catatonic schizophrenia: diagnostic and treatment issues
P I Rosebush, G M MacQueen, J T Clarke, et al.
Biochemical Medicine and Metabolic Biology
|
October 1, 1994
Homozygous presence of the crossover (fusion gene) mutation identified in a type II Gaucher disease fetus: is this analogous to the Gaucher knock-out mouse model?
P M Strasberg, M A Skomorowski, I B Warren, et al.
Journal of Clinical Laboratory Analysis
|
January 1, 1994
Genotype-phenotype pitfalls in Gaucher disease
P M Strasberg, B L Triggs-Raine, I B Warren, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Canadian Journal of Biochemistry
|
June 1, 1979
Binding of mitochondrial malate dehydrogenase to mitoplasts
P M Strasberg, K A Webster, H V Patel, et al.
Biochemical Genetics
|
August 1, 1979
Mitochondrial malic enzyme in mosaic skeletal muscle of mouse chimeras
P M Frair, P M Strasberg, K B Freeman, et al.
American Journal of Human Genetics
|
August 1, 1991
Hunter disease (mucopolysaccharidosis type II) associated with unbalanced inactivation of the X chromosomes in a karyotypically normal girl
J T Clarke, W L Greer, P M Strasberg, et al.
The Journal of Clinical Psychiatry
|
August 1, 1995
Late-onset Tay-Sachs disease presenting as catatonic schizophrenia: diagnostic and treatment issues
P I Rosebush, G M MacQueen, J T Clarke, et al.
Biochemical Medicine and Metabolic Biology
|
October 1, 1994
Homozygous presence of the crossover (fusion gene) mutation identified in a type II Gaucher disease fetus: is this analogous to the Gaucher knock-out mouse model?
P M Strasberg, M A Skomorowski, I B Warren, et al.
Journal of Clinical Laboratory Analysis
|
January 1, 1994
Genotype-phenotype pitfalls in Gaucher disease
P M Strasberg, B L Triggs-Raine, I B Warren, et al.
Page
of 2