A genetic study of a defect in glutathione metabolism of the erythrocyte.
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Biochemical Phenomena↗
Biomedical subjects
B CHILDS
Publications and source records attributed to B CHILDS.
A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.
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Erythrocytes↗
Genetic aspects of congenital metabolic disease.
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Heredity↗
A defect of glutathione metabolism in erythrocytes from patients with a naphthalene-induced hemolytic anemia.
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Anemia↗
A survey of genetics as it applies to problems in medicine.
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Data Collection↗
Virilizing adrenal hyperplasia; a genetic and hormonal study.
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Adrenal Cortex↗
Familial nonhemolytic jaundice with kernicterus; a report of two cases without neurologic damage.
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Child↗
The nature of direct bilirubin.
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Bilirubin↗
Birth weights of children with cerebral palsy.
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Birth Weight↗
Etiologic factors cases.
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Congenital Hypothyroidism↗
The crystallization and properties of serum bilirubin.
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Bilirubin↗
Urinary excretion of free alpha-amino acid nitrogen by normal infants and children.
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Amino Acids↗