The genetics of glutamic-pyruvic transaminase in mice: inheritance, electrophoretic phenotypes, and postnatal changes.
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Alanine Transaminase↗
Biomedical subjects
C R Scott
Publications and source records attributed to C R Scott.
A mucopolysaccharide storage disease with involvement of the renal glomerular epithelium.
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Autopsy↗
-Galactosidase, N-acetyl- -glucosaminidase, and -glucuronidase activity in fibroblast cultures from patients with mucopolysaccharide storage disease.
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Adult↗
X-linked transmission of ornithine-transcarbamylase deficiency.
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Humans↗
Hereditary transcobalamin II deficiency: the role of transcobalamin II in vitamin B 12 -mediated reactions.
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Amino Acid Metabolism, Inborn Errors↗
Amino acids in amniotic fluid: changes in concentrations during the first half of pregnancy.
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Abortion, Therapeutic↗
Syndrome of accelerated skeletal maturation and relative failure to thrive: a newly recognized clinical growth disorder.
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Age Determination by Skeleton↗
A new craniodigital syndrome with mental retardation.
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Abnormalities, Multiple↗
Accuracy of cardiac output computers.
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Animals↗
Clinical and cellular studies of sarcosinemia.
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Amino Acid Metabolism, Inborn Errors↗
Cystathioninemia: a benign genetic condition.
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Adolescent↗
Hemodynamic effectiveness of colloid and electrolyte solutions for replacement of simulated operative blood loss.
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Acid-Base Equilibrium↗
Arylamino alcohol antimalarials. A new method for incorporating the side chain.
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Amino Alcohols↗
Familial neurovisceral lipidosis.
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Bone and Bones↗
A rapid assay for urinary porphyrins by thin-layer chromatography.
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Alcohols↗
Hereditary leukokeratosis, white mouth.
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Adult↗
Urinary N-sulfate glycosaminoglycan excretion in children: normal and abnormal values.
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Abnormalities, Multiple↗
Hypertrophied frenuli, oligophrenia, familial trembling and anomalies of the hand. Report of four cases in one family and a forme fruste in another.
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Congenital Abnormalities↗