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American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1969 May;21(3):285–289.

The distribution of genetic polymorphisms among patients with Down's syndrome, phenylketonuria, and cystic fibrosis of the pancreas.

D Y Hsia, L Y Shih, S Easterberg, J Farquhar, C B Kim, S Yeh, A Young
PMCID: PMC1706415  PMID: 4240106

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Selected References

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

  1. BECKMAN L. A typical haptoglobin patterns in tumour patients. Lancet. 1959 Nov 28;2(7109):952–953. doi: 10.1016/s0140-6736(59)91593-4. [DOI] [PubMed] [Google Scholar]
  2. BOYER S. H., FAINER D. C., WATSON-WILLIAMS E. J. Lactate dehydrogenase variant from human blood: evidence for molecular subunits. Science. 1963 Aug 16;141(3581):642–643. doi: 10.1126/science.141.3581.642. [DOI] [PubMed] [Google Scholar]
  3. Bowman J. E., Carson P. E., Frischer H., De Garay A. L. Genetics of starch-gel electrophoretic variants of human 6-phosphogluconic dehydrogenase: population and family studies in the United States and in Mexico. Nature. 1966 May 21;210(5038):811–813. doi: 10.1038/210811a0. [DOI] [PubMed] [Google Scholar]
  4. Bowman J. E., Frischer H., Ajmar F., Carson P. E., Gower M. K. Population, family and biochemical investigation of human adenylate kinase polymorphism. Nature. 1967 Jun 10;214(5093):1156–1158. doi: 10.1038/2141156a0. [DOI] [PubMed] [Google Scholar]
  5. ERIKSSON S. PULMONARY EMPHYSEMA AND ALPHA1-ANTITRYPSIN DEFICIENCY. Acta Med Scand. 1964 Feb;175:197–205. doi: 10.1111/j.0954-6820.1964.tb00567.x. [DOI] [PubMed] [Google Scholar]
  6. HOPKINSON D. A., SPENCER N., HARRIS H. RED CELL ACID PHOSPHATASE VARIANTS: A NEW HUMAN POLYMORPHISM. Nature. 1963 Sep 7;199:969–971. doi: 10.1038/199969a0. [DOI] [PubMed] [Google Scholar]
  7. Jörgensen G., Hempel D. Die Verteilung der Gc-Phänotypen und Gc-Allele bei der Tuberkulose. Humangenetik. 1968;6(1):74–77. doi: 10.1007/BF00287157. [DOI] [PubMed] [Google Scholar]
  8. KIRKMAN H. N., HENDRICKSON E. M. Sex-linked electrophoretic difference in glucose-6-phosphate dehydrogenase. Am J Hum Genet. 1963 Sep;15:241–258. [PMC free article] [PubMed] [Google Scholar]
  9. MITCHELL J., HALDEN E. R., JONES F., BRYAN S., STIRMAN J. A., MUIRHEAD E. E. Lowering of transferrin during iron absorption in iron deficiency. J Lab Clin Med. 1960 Oct;56:555–569. [PubMed] [Google Scholar]
  10. NOSSLIN B. F., NYMAN M. Haptoglobin determination in diagnosis of haemolytic diseases. Lancet. 1958 May 10;1(7028):1000–1001. doi: 10.1016/s0140-6736(58)91804-x. [DOI] [PubMed] [Google Scholar]
  11. PEACOCK A. C., BUNTING S. L., QUEEN K. G. SERUM PROTEIN ELECTROPHORESIS IN ACRYLAMIDE GEL: PATTERNS FROM NORMAL HUMAN SUBJECTS. Science. 1965 Mar 19;147(3664):1451–1453. doi: 10.1126/science.147.3664.1451. [DOI] [PubMed] [Google Scholar]
  12. SALZANO F. M., HIRSCHFELD H. THE DYNAMICS OF THE GC POLYMORPHISM IN A BRAZILIAN POPULATION. Acta Genet Stat Med. 1965;15:116–125. doi: 10.1159/000151899. [DOI] [PubMed] [Google Scholar]
  13. SPENCER N., HOPKINSON D. A., HARRIS H. PHOSPHOGLUCOMUTASE POLYMORPHISM IN MAN. Nature. 1964 Nov 21;204:742–745. doi: 10.1038/204742a0. [DOI] [PubMed] [Google Scholar]
  14. Schwantes A. R., Salzano F. M., De Castro I. V., Tondo C. V. Haptoglobins and leprosy. Acta Genet Stat Med. 1967;17(1):127–136. doi: 10.1159/000152060. [DOI] [PubMed] [Google Scholar]

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