Search research articles
Contact Us
Filters
Showing results (21-30 of 98) with videos related to
Page
of 10
Sort By:
American Journal of Human Genetics
|
October 1, 1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase
J K Reichardt, S Packman, S L Woo
Neurology
|
August 1, 1982
Brain pyruvate carboxylase and the pathophysiology of biotin-dependent diseases
J E Sander, S Packman, J J Townsend
European Journal of Respiratory Diseases. Supplement
|
January 1, 1983
Response to almitrine bismesylate in a child with a central alveolar hypoventilation syndrome
C J Newth, S Packman, R T Bachand
Biochemical and Biophysical Research Communications
|
November 1, 1972
A comparison of globin genes in duck reticulocytes and liver cells
S Packman, H Aviv, J Ross, et al.
Journal of the American Academy of Dermatology
|
July 1, 1983
Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiency
M L Williams, S Packman, M J Cowan
Journal of Inherited Metabolic Disease
|
January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosis
A Seyda, K Chun, S Packman, et al.
The Journal of Clinical Investigation
|
May 1, 1987
Metallothionein messenger RNA regulation in the mottled mouse and Menkes kinky hair syndrome
S Packman, R D Palmiter, M Karin, et al.
The Journal of Biological Chemistry
|
September 25, 1978
Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunits
J Kraus, S Packman, B Fowler, et al.
The Journal of Clinical Investigation
|
March 1, 1978
Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts
B Fowler, J Kraus, S Packman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 98) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
October 1, 1991
Molecular characterization of two galactosemia mutations: correlation of mutations with highly conserved domains in galactose-1-phosphate uridyl transferase
J K Reichardt, S Packman, S L Woo
Neurology
|
August 1, 1982
Brain pyruvate carboxylase and the pathophysiology of biotin-dependent diseases
J E Sander, S Packman, J J Townsend
European Journal of Respiratory Diseases. Supplement
|
January 1, 1983
Response to almitrine bismesylate in a child with a central alveolar hypoventilation syndrome
C J Newth, S Packman, R T Bachand
Biochemical and Biophysical Research Communications
|
November 1, 1972
A comparison of globin genes in duck reticulocytes and liver cells
S Packman, H Aviv, J Ross, et al.
Journal of the American Academy of Dermatology
|
July 1, 1983
Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiency
M L Williams, S Packman, M J Cowan
Journal of Inherited Metabolic Disease
|
January 5, 2002
A case of PDH-E1 alpha mosaicism in a male patient with severe metabolic lactic acidosis
A Seyda, K Chun, S Packman, et al.
The Journal of Clinical Investigation
|
May 1, 1987
Metallothionein messenger RNA regulation in the mottled mouse and Menkes kinky hair syndrome
S Packman, R D Palmiter, M Karin, et al.
The Journal of Biological Chemistry
|
September 25, 1978
Purification and properties of cystathionine beta-synthase from human liver. Evidence for identical subunits
J Kraus, S Packman, B Fowler, et al.
The Journal of Clinical Investigation
|
March 1, 1978
Homocystinuria. Evidence for three distinct classes of cystathionine beta-synthase mutants in cultured fibroblasts
B Fowler, J Kraus, S Packman, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism
C Jakobs, L Sweetman, W L Nyhan, et al.
Page
of 10