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Phenotypes of Galactosaemia in Infants Screened at Birth

Five genetic forms of galactosaemia were found in 15 infants identified in a newborn screening programme through a combination of laboratory criteria, involving serial assays of transferase and interpretation of isozyme patterns. The biochemical phenotypes of some infants were ascertained only weeks...

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Detalhes bibliográficos
Main Authors: Kelly, Sally, Desjardins, Lucille, Armerding, Paul, Burns, Jean
Formato: Artigo
Idioma:Inglês
Publicado em: 1973
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1012972/
https://ncbi.nlm.nih.gov/pubmed/4697852
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