Biomedical subjects
D Y HSIA
Publications and source records attributed to D Y HSIA.
Development of 5-hydroxytryptophan decarboxylase activity in rat kidney.
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The genetic mechanism of galactosaemia.
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Recent developments in inborn errors of metabolism.
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Further studies on the heterozygous carrier in galactosemia.
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Recent advances in biochemical detection of heterozygous carriers in hereditary diseases.
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Studies on linkage between phenylketonuria and the blood groups.
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Activity of glucose-6-phosphate dehydrogenase in erythrocyes of patients with various abnormal hemoglobins.
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Detection of heterozygous carriers in glycogen storage disease of the liver (von Gierke's disease).
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Studies on the genetic mechanism of cystic fibrosis of the pancreas.
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Birth weight in cystic fibrosis of the pancreas.
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Sodium glucuronate and glucuronolactone in bilirubin conjugation and formation of borneol glucuronide.
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An inborn error of lipid metabolism.
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Studies on the heterozygous carrier in galactosemia.
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Experimental studies on blood-spinal fluid barrier for bilirubin.
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The heterozygous carrier in galactosaemia.
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Prolonged obstructive jaundice in infancy. V. The genetic components in neonatal hepatitis.
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A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria.
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