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Journal of Nutritional Science and Vitaminology
|
December 1, 1991
Biotin transport in the rat central nervous system
W Lo, T Kadlecek, S Packman
Nature Genetics
|
July 1, 1997
Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse
B Levinson, S Packman, J Gitschier
The Surgical Clinics of North America
|
June 1, 1995
Indications for parathyroidectomy and extent of treatment for patients with secondary hyperparathyroidism
K S Packman, M J Demeure
Human Molecular Genetics
|
July 1, 1997
Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters
Y M Kuo, J Gitschier, S Packman
Journal of Inherited Metabolic Disease
|
November 20, 2009
Psychological aspects of patients with Fabry disease
T Wilson Crosbie, Wendy Packman, S Packman
Biochemical Genetics
|
February 1, 1982
Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiency
S Packman, N M Caswell, H Baker
Advances in Experimental Medicine and Biology
|
March 18, 1999
Developmental expression of the mouse mottled and toxic milk genes
Y M Kuo, J Gitschier, S Packman
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
April 28, 2001
Hyperammonemia in urea cycle disorders: role of the nephrologist
R S Mathias, D Kostiner, S Packman
The Journal of Pediatrics
|
September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiency
S Packman, L Sweetman, H Baker, et al.
American Journal of Medical Genetics
|
November 1, 1992
Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosis
L Ferrell, K Schmidt, V Sheffield, et al.
Page
of 10
Search research articles
Search
Showing results (11-20 of 98) with videos related to
Sort By:
Page
of 10
Journal of Nutritional Science and Vitaminology
|
December 1, 1991
Biotin transport in the rat central nervous system
W Lo, T Kadlecek, S Packman
Nature Genetics
|
July 1, 1997
Deletion of the promoter region in the Atp7a gene of the mottled dappled mouse
B Levinson, S Packman, J Gitschier
The Surgical Clinics of North America
|
June 1, 1995
Indications for parathyroidectomy and extent of treatment for patients with secondary hyperparathyroidism
K S Packman, M J Demeure
Human Molecular Genetics
|
July 1, 1997
Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transporters
Y M Kuo, J Gitschier, S Packman
Journal of Inherited Metabolic Disease
|
November 20, 2009
Psychological aspects of patients with Fabry disease
T Wilson Crosbie, Wendy Packman, S Packman
Biochemical Genetics
|
February 1, 1982
Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiency
S Packman, N M Caswell, H Baker
Advances in Experimental Medicine and Biology
|
March 18, 1999
Developmental expression of the mouse mottled and toxic milk genes
Y M Kuo, J Gitschier, S Packman
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
April 28, 2001
Hyperammonemia in urea cycle disorders: role of the nephrologist
R S Mathias, D Kostiner, S Packman
The Journal of Pediatrics
|
September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiency
S Packman, L Sweetman, H Baker, et al.
American Journal of Medical Genetics
|
November 1, 1992
Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosis
L Ferrell, K Schmidt, V Sheffield, et al.
Page
of 10