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Family Medicine
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November 1, 1991
Populations at risk for drug-related admissions
R R Howell, K W Jones
Science (New York, N.Y.)
|
April 28, 1989
Hydrogen Sulfide on IO: Evidence from Telescopic and Laboratory Infrared Spectra
D B Nash, R R Howell
Biochimica Et Biophysica Acta
|
February 28, 1977
Genetic evidence for the common identity of glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase
P M Hefferan, R R Howell
Family Medicine
|
February 1, 1993
Prescription-writing errors and markers: the value of knowing the diagnosis
R R Howell, K W Jones
Monographs in Human Genetics
|
January 1, 1978
Copper metabolism in Menkes disease
T J Goka, R R Howell
Clinical Genetics
|
December 1, 1985
Ectodermal manifestations in Menkes disease
C M Moore, R R Howell
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 1, 1972
Arylsulfatase A activity in human urine: quantitative studies on patients with lysosomal disorders including metachromatic leukodystrophy
G H Thomas, R R Howell
The Journal of Pediatrics
|
July 1, 1972
Galactokinase deficiency: clinical and biochemical findings in a new kindred
W R Pickering, R R Howell
Birth Defects Original Article Series
|
February 1, 1971
Generalized gangliosidosis
R R Howell, E E Lippman
The New England Journal of Medicine
|
June 11, 1970
Infantile metachromatic leukodystrophy
M M Kaback, R R Howell
Page
of 7
Search research articles
Search
Showing results (21-30 of 67) with videos related to
Sort By:
Page
of 7
Family Medicine
|
November 1, 1991
Populations at risk for drug-related admissions
R R Howell, K W Jones
Science (New York, N.Y.)
|
April 28, 1989
Hydrogen Sulfide on IO: Evidence from Telescopic and Laboratory Infrared Spectra
D B Nash, R R Howell
Biochimica Et Biophysica Acta
|
February 28, 1977
Genetic evidence for the common identity of glucose-6-phosphatase, pyrophosphate-glucose phosphotransferase, carbamyl phosphate-glucose phosphotransferase and inorganic pyrophosphatase
P M Hefferan, R R Howell
Family Medicine
|
February 1, 1993
Prescription-writing errors and markers: the value of knowing the diagnosis
R R Howell, K W Jones
Monographs in Human Genetics
|
January 1, 1978
Copper metabolism in Menkes disease
T J Goka, R R Howell
Clinical Genetics
|
December 1, 1985
Ectodermal manifestations in Menkes disease
C M Moore, R R Howell
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
January 1, 1972
Arylsulfatase A activity in human urine: quantitative studies on patients with lysosomal disorders including metachromatic leukodystrophy
G H Thomas, R R Howell
The Journal of Pediatrics
|
July 1, 1972
Galactokinase deficiency: clinical and biochemical findings in a new kindred
W R Pickering, R R Howell
Birth Defects Original Article Series
|
February 1, 1971
Generalized gangliosidosis
R R Howell, E E Lippman
The New England Journal of Medicine
|
June 11, 1970
Infantile metachromatic leukodystrophy
M M Kaback, R R Howell
Page
of 7