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. 1970 Jul;85(7):575–578.

Screening for galactosemia in New York State.

S Kelly, S Katz, J Burns, J Boylan
PMCID: PMC2031674  PMID: 4987471

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BEUTLER E., BALUDA M., DONNELL G. N. A NEW METHOD FOR THE DETECTION OF GALACTOXEMIA AND ITS CARRIER STATE. J Lab Clin Med. 1964 Oct;64:694–705. [PubMed] [Google Scholar]
  2. BEUTLER E., DAY R., BALUDA M., POLK K. SCREENING FOR GALACTOSEMIA AMONG MENTALLY RETARDED PATIENTS. J Ment Defic Res. 1965 Mar;9:61–68. doi: 10.1111/j.1365-2788.1965.tb00821.x. [DOI] [PubMed] [Google Scholar]
  3. Beutler E. A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency. Blood. 1966 Oct;28(4):553–562. [PubMed] [Google Scholar]
  4. Beutler E., Baluda M. C. A simple spot screening test for galactosemia. J Lab Clin Med. 1966 Jul;68(1):137–141. [PubMed] [Google Scholar]
  5. Beutler E., Baluda M. C., Sturgeon P., Day R. W. The genetics of galactose-1-phosphate uridyl transferase deficiency. J Lab Clin Med. 1966 Oct;68(4):646–658. [PubMed] [Google Scholar]
  6. Beutler E., Irwin H. R., Blumenfeld C. M., Goldenburg E. W., Day R. W. Field test of galactosemia screening methods in newborn infants. JAMA. 1967 Feb 13;199(7):501–503. [PubMed] [Google Scholar]
  7. Beutler E., Mitchell M. New rapid method for the estimation of red cell galactose-1-phosphate uridyl transferase activity. J Lab Clin Med. 1968 Sep;72(3):527–532. [PubMed] [Google Scholar]
  8. Brandt N. J. Frequency of heterozygotes for hereditary galactosaemia in a normal population. Acta Genet Stat Med. 1967;17(4):289–298. doi: 10.1159/000152075. [DOI] [PubMed] [Google Scholar]
  9. HANSEN R. G., BRETTHAUER R. K., MAYES J., NORDIN J. H. ESTIMATION OF FREQUENCY OF OCCURRENCE OF GALACTOSEMIA IN THE POPULATION. Proc Soc Exp Biol Med. 1964 Feb;115:560–563. doi: 10.3181/00379727-115-28968. [DOI] [PubMed] [Google Scholar]
  10. Haworth J. C., Barchuk N. H. A simple chromatographic screening test for the detection of galactosemia in newborn infants. Pediatrics. 1967 Apr;39(4):608–610. [PubMed] [Google Scholar]
  11. Hsia D. Y. Clinical variants of galactosemia. Metabolism. 1967 May;16(5):419–437. doi: 10.1016/0026-0495(67)90133-3. [DOI] [PubMed] [Google Scholar]
  12. LONDON M., MARYMONT J. H., Jr, FULD J. A MICRODIFFUSION TEST FOR CONGENITAL GALACTOSEMIA UTILIZING GALACTOSE-1-C14. Pediatrics. 1964 Mar;33:421–424. [PubMed] [Google Scholar]
  13. Mathai C. K., Beutler E. Electrophoretic variation of galactose-1-phosphate uridyltransferase. Science. 1966 Dec 2;154(3753):1179–1180. doi: 10.1126/science.154.3753.1179. [DOI] [PubMed] [Google Scholar]
  14. ROBERTSON A. F. CASE REPORT: THE COINCIDENCE OF BILIARY ATRESIA AND THE HETEROZYGOUS STATE OF GALACTOSEMIA. Pediatrics. 1965 Jun;35:1008–1010. [PubMed] [Google Scholar]
  15. ROBINSON A. THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT. J Exp Med. 1963 Sep 1;118:359–370. doi: 10.1084/jem.118.3.359. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. SCHWARZ V., WELLS A. R., HOLZEL A., KOMROWER G. M. A study of the genetics of galactosaemia. Ann Hum Genet. 1961 Dec;25:179–188. doi: 10.1111/j.1469-1809.1962.tb01518.x. [DOI] [PubMed] [Google Scholar]

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