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American Journal of Medical Genetics
|
April 1, 1982
Phenylalanine levels in PKU following minor surgery
A E Fiedler, M J Miller, H Bickel, et al.
American Journal of Mental Deficiency
|
January 1, 1973
Argininosuccinic aciduria
S D Cederbaum, K N Shaw, M Valente, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1994
Inclusion of synthetic DNA templates of similar length and base composition to PCR-amplified products in restriction enzyme digestions: an efficient aid in characterization of point mutations
D Klein, D E Tabor, R Z Sokol, et al.
The Journal of Pediatrics
|
November 1, 1976
The chondro-osseous dysplasia of adenosine deaminase deficiency with severe combined immunodeficiency
S D Cederbaum, I Kaitila, D L Rimoin, et al.
Clinical Chemistry
|
July 1, 1992
Pitfalls of restriction endonuclease digestion for direct detection of point mutations
D Klein, W W Grody, D E Tabor, et al.
The Journal of Urology
|
August 28, 1998
Voiding dysfunction in a mother and daughter with mitochondrial cytopathy
M H Safir, A E Gousse, S D Cederbaum, et al.
The Western Journal of Medicine
|
August 1, 1984
Recombinant DNA in medicine
S D Cederbaum, G C Fareed, M A Lovett, et al.
Monographs in Human Genetics
|
January 1, 1978
Pyruvate dehydrogenase deficiency in 35 patients
J P Blass, S D Cederbaum, R A Kark, et al.
Molecular and Cellular Biochemistry
|
February 1, 1985
Differential expression of multiple forms of arginase in cultured cells
E B Spector, R M Kern, D F Haggerty, et al.
Biochemical and Biophysical Research Communications
|
November 26, 1986
Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genes
G J Dizikes, W W Grody, R M Kern, et al.
Page
of 10
Search research articles
Search
Showing results (31-40 of 93) with videos related to
Sort By:
Page
of 10
American Journal of Medical Genetics
|
April 1, 1982
Phenylalanine levels in PKU following minor surgery
A E Fiedler, M J Miller, H Bickel, et al.
American Journal of Mental Deficiency
|
January 1, 1973
Argininosuccinic aciduria
S D Cederbaum, K N Shaw, M Valente, et al.
Somatic Cell and Molecular Genetics
|
January 1, 1994
Inclusion of synthetic DNA templates of similar length and base composition to PCR-amplified products in restriction enzyme digestions: an efficient aid in characterization of point mutations
D Klein, D E Tabor, R Z Sokol, et al.
The Journal of Pediatrics
|
November 1, 1976
The chondro-osseous dysplasia of adenosine deaminase deficiency with severe combined immunodeficiency
S D Cederbaum, I Kaitila, D L Rimoin, et al.
Clinical Chemistry
|
July 1, 1992
Pitfalls of restriction endonuclease digestion for direct detection of point mutations
D Klein, W W Grody, D E Tabor, et al.
The Journal of Urology
|
August 28, 1998
Voiding dysfunction in a mother and daughter with mitochondrial cytopathy
M H Safir, A E Gousse, S D Cederbaum, et al.
The Western Journal of Medicine
|
August 1, 1984
Recombinant DNA in medicine
S D Cederbaum, G C Fareed, M A Lovett, et al.
Monographs in Human Genetics
|
January 1, 1978
Pyruvate dehydrogenase deficiency in 35 patients
J P Blass, S D Cederbaum, R A Kark, et al.
Molecular and Cellular Biochemistry
|
February 1, 1985
Differential expression of multiple forms of arginase in cultured cells
E B Spector, R M Kern, D F Haggerty, et al.
Biochemical and Biophysical Research Communications
|
November 26, 1986
Isolation of human liver arginase cDNA and demonstration of nonhomology between the two human arginase genes
G J Dizikes, W W Grody, R M Kern, et al.
Page
of 10