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Major Problems in Clinical Pediatrics
|
January 1, 1973
Amino acid metabolism and its disorders
C R Scriver, L E Rosenberg
Annual Review of Genetics
|
January 1, 1980
Phenylketonuria and other phenylalanine hydroxylation mutants in man
C R Scriver, C L Clow
Canadian Journal of Biochemistry
|
June 1, 1978
The defect in transcellular transport of phosphate in the nephron is located in brush-border membranes in X-linked hypophosphatemia (Hyp mouse model)
H S Tenenhouse, C R Scriver
L'Union Medicale Du Canada
|
January 1, 1993
[Genetics in medicine: the 5th decade in Québec]
C M Laberge, C R Scriver
Journal of Inherited Metabolic Disease
|
January 1, 1992
X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosage
C R Scriver, H S Tenenhouse
Lancet (London, England)
|
October 17, 1987
Renal hypophosphataemia has several mendelian forms
C R Scriver, T M Reade
The Journal of Pediatrics
|
September 1, 1988
Avoiding phenylketonuria: why parents seek prenatal diagnosis
C R Scriver, C L Clow
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 23, 1980
Age-dependent serum sulfate levels in children and adolescents
D E Cole, C R Scriver
Endocrinology
|
August 1, 1981
Effect of 1,25-dihydroxyvitamin D3 on phosphate homeostasis in the X-linked hypophosphatemic (Hyp) mouse
H S Tenenhouse, C R Scriver
The New England Journal of Medicine
|
June 14, 1979
Hypophosphatemic rickets and breast milk
T M Reade, C R Scriver
Page
of 32
Search research articles
Search
Showing results (101-110 of 317) with videos related to
Sort By:
Page
of 32
Major Problems in Clinical Pediatrics
|
January 1, 1973
Amino acid metabolism and its disorders
C R Scriver, L E Rosenberg
Annual Review of Genetics
|
January 1, 1980
Phenylketonuria and other phenylalanine hydroxylation mutants in man
C R Scriver, C L Clow
Canadian Journal of Biochemistry
|
June 1, 1978
The defect in transcellular transport of phosphate in the nephron is located in brush-border membranes in X-linked hypophosphatemia (Hyp mouse model)
H S Tenenhouse, C R Scriver
L'Union Medicale Du Canada
|
January 1, 1993
[Genetics in medicine: the 5th decade in Québec]
C M Laberge, C R Scriver
Journal of Inherited Metabolic Disease
|
January 1, 1992
X-linked hypophosphataemia: a homologous phenotype in humans and mice with unusual organ-specific gene dosage
C R Scriver, H S Tenenhouse
Lancet (London, England)
|
October 17, 1987
Renal hypophosphataemia has several mendelian forms
C R Scriver, T M Reade
The Journal of Pediatrics
|
September 1, 1988
Avoiding phenylketonuria: why parents seek prenatal diagnosis
C R Scriver, C L Clow
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 23, 1980
Age-dependent serum sulfate levels in children and adolescents
D E Cole, C R Scriver
Endocrinology
|
August 1, 1981
Effect of 1,25-dihydroxyvitamin D3 on phosphate homeostasis in the X-linked hypophosphatemic (Hyp) mouse
H S Tenenhouse, C R Scriver
The New England Journal of Medicine
|
June 14, 1979
Hypophosphatemic rickets and breast milk
T M Reade, C R Scriver
Page
of 32