The genetics of galactose-1-phosphate uridyl transferase deficiency.
about
Galactosemia: a strategy to identify new biochemical phenotypes and molecular genotypesGenic variation within and between the three major races of man, Caucasoids, Negroids, and Mongoloids'Durate variant with clinical signs' has alpha1 -antitrypsin genotype ZZ.Experience of routine live-birth screening for galactosaemia in a British hospital, with emphasis on heterozygote detectionTwo more "private" polymorphisms of Amerindian tribes: LDHb GUA-1 and ACP1 B GUA-1 in the Guaymi in Panama.Human erythrocyte galactokinase and galactose-1-phosphate uridylyltransferase: a population survey.Screening for galactosemia in New York StateGalactose-1-phosphate uridyltransferase and galactokinase activity in cultured human diploid fibroblasts and peripheral blood leukocytes. I. Analysis of transferase genotypes by the ratio of the activities of the two enzymes.Phenotypes of galactosaemia in infants screened at birth.Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
P2860
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P2860
The genetics of galactose-1-phosphate uridyl transferase deficiency.
description
1966 nî lūn-bûn
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1966年の論文
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1966年学术文章
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1966年学术文章
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1966年学术文章
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1966年学术文章
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1966年学术文章
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1966年学术文章
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1966年學術文章
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1966年學術文章
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name
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@en
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@nl
type
label
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@en
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@nl
prefLabel
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@en
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@nl
P2093
P1476
The genetics of galactose-1-phosphate uridyl transferase deficiency.
@en
P2093
P304
P577
1966-10-01T00:00:00Z