SEX DIFFERENCES IN SUSCEPTIBILITY TO INFECTIONS.
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Adolescent↗
Biomedical subjects
B CHILDS
Publications and source records attributed to B CHILDS.
GENETIC ORIGIN OF SOME SEX DIFFERENCES AMONG HUMAN BEINGS.
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Agammaglobulinemia↗
GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN DROSOPHILA: X-LINKED ELECTROPHORETIC VARIANTS.
Three electrophoretic patterns of glucose-6-phosphate dehydrogenase have been found in wild-type strains of Drosophila melanogaster. Genetical control of the variants in enzyme mobility (fast or slow) is X-linked; strains possessing both bands (fast and slow) appear to be heterogeneous, having individuals of three types (fast, slow, and double).
Animals↗
GENETIC VARIATIONS IN THE QUANTITATIVE CONTROL OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY.
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Black People↗
HYPERGLYCINEMIA. V. THE MISCIBLE POOL AND TURNOVER RATE OF GLYCINE AND THE FORMATION OF SERINE.
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Amino Acid Metabolism, Inborn Errors↗
FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA.
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Acidosis↗
GENETIC IMPLICATIONS OF RARE DISEASES.
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Eugenics↗
Genetic variations in man.
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Genetic Variation↗
DEMONSTRATION OF TWO POPULATIONS OF CELLS IN THE HUMAN FEMALE HETEROZYGOUS FOR GLUCOSE-6-PHOSPHATE DEHYDROGENASE VARIANTS.
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Chromosomes↗
Dosage compensation in the regulation of erythrocyte glucose-6-phosphate dehydrogenase activity.
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Chromosomes↗
Observations on sex differences in human biology.
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Humans↗
Principles of modern genetics.
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Genetics, Medical↗
Primaquine sensitivity of erythrocytes.
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Anemia↗
Idiopathic hyperglycinemia and hyperglycinuria: a new disorder of amino acid metabolism. I.
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Amino Acid Metabolism, Inborn Errors↗
Idiopathic hyperglycinemia: a new disorder of amino acid metabolism. II. The concentrations of other amino acids in the plasma and their modification by the administration of leucine.
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Amino Acid Metabolism, Inborn Errors↗
Genetics and metabolism.
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Genetics, Medical↗
Hereditary aspects of disease.
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Disease↗
Glucuronic acid conjugation by patients with familial nonhemolytic jaundice and their relatives.
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Child↗