Problems in the Diagnosis of Hereditary Galactosaemia
- 21 January 1967
- journal article
- review article
- Published by Wiley in Acta Paediatrica
- Vol. 56 (1), 85-96
- https://doi.org/10.1111/j.1651-2227.1967.tb15347.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCYThe Lancet, 1965
- Studies on Tyrosinosis: 1, Effect of Low-tyrosine and Low-phenylalanine DietBMJ, 1964
- A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTSPediatrics, 1963
- A study of the genetics of galactosaemiaAnnals of Human Genetics, 1962
- Variability in the clinical manifestations of galactosemiaThe Journal of Pediatrics, 1961
- Growth and development of children with galactosemiaThe Journal of Pediatrics, 1961
- The Genetic Mechanism of GalactosaemiaArchives of Disease in Childhood, 1960
- The Value of Galactose Phosphate Determinations in the treatment of GalactosaemiaArchives of Disease in Childhood, 1960
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956
- GalactosaemiaActa Paediatrica, 1955