Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
. 1966 Sep;3(3):198–202. doi: 10.1136/jmg.3.3.198

Genetic diversity in serum albumin.

M S Adams
PMCID: PMC1012939  PMID: 5971057

Full text

PDF
198

Images in this article

Selected References

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

  1. ADNER P. L., REDFORS A. [A family with 2 albumin fractions (bisalbuminemia) determined by serum electrophoresis]. Nord Med. 1961 May 4;65:623–625. [PubMed] [Google Scholar]
  2. ASHTON G. C., LAMPKIN G. H. SERUM ALBUMIN AND TRANSFERRIN POLYMORPHISM IN EAST AFRICAN CATTLE. Nature. 1965 Jan 9;205:209–210. [PubMed] [Google Scholar]
  3. BERGSTRAND C. G., CZAR B. Paper electrophoretic study of human fetal serum proteins with demonstration of a new protein fraction. Scand J Clin Lab Invest. 1957;9(3):277–286. doi: 10.3109/00365515709079971. [DOI] [PubMed] [Google Scholar]
  4. Braend M., Efremov G., Fagerhol M. K., Hartmann O. Albumin and transferrin variants in Norwegians. Hereditas. 1965;53(1):137–142. doi: 10.1111/j.1601-5223.1965.tb01986.x. [DOI] [PubMed] [Google Scholar]
  5. EARLE D. P., HUTT M. P., SCHMID K., GITLIN D. Observations on double albumin: a genetically transmitted serum protein anomaly. J Clin Invest. 1959 Aug;38(8):1412–1420. doi: 10.1172/JCI103917. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. EFREMOV G., BRAEND M. SERUM ALBUMIN: POLYMORPHISM IN MAN. Science. 1964 Dec 25;146(3652):1679–1680. doi: 10.1126/science.146.3652.1679. [DOI] [PubMed] [Google Scholar]
  7. FRANGLEN G., MARTIN N. H., HARGREAVES T., SMITH M. J., WILLIAMS D. I. Bisalbuminaemia: a hereditary albumin abnormality. Lancet. 1960 Feb 6;1(7119):307–308. doi: 10.1016/s0140-6736(60)90237-3. [DOI] [PubMed] [Google Scholar]
  8. GITLIN D., SCHMID K., EARLE D. P., GIVERLBER H. Observations on double albumin. II. A peptide difference between two genetically determined human serum albumins. J Clin Invest. 1961 May;40:820–827. doi: 10.1172/JCI104315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GOODMAN M. Evolution of the immunologic species specificity of human serum proteins. Hum Biol. 1962 May;34:104–150. [PubMed] [Google Scholar]
  10. HALEY L. E. SERUM ALBUMIN POLYMORPHISM IN QUAIL AND CHICKEN-QUAIL HYBRIDS. Genetics. 1965 Jun;51:983–986. doi: 10.1093/genetics/51.6.983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. KNEDEL M. Die Doppel-Albuminämie, eine neue erbliche Proteinanomalie. Blut. 1957 May;3(3):129–134. doi: 10.1007/BF01630687. [DOI] [PubMed] [Google Scholar]
  12. NENNSTIEL H. J., BECHT T. Uber das erbliche Auftreten einer Albuminspaltung im Elektrophoresedlagramm. Klin Wochenschr. 1957 Jul 1;35(13):689–689. doi: 10.1007/BF01481274. [DOI] [PubMed] [Google Scholar]
  13. QUINTEROS I. R., STEVENS R. W., STORMONT C., ASMUNDSON V. S. ALBUMIN PHENOTYPES IN TURKEYS. Genetics. 1964 Oct;50:579–582. doi: 10.1093/genetics/50.4.579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. ROBBINS J. L., HILL G. A., MARCUS S., CARLQUIST J. H. PARALBUMINEMIA: PAPER AND CELLULOSE ACETATE ELECTROPHORESIS AND PRELIMINARY IMMUNOELECTROPHORETIC ANALYSIS. J Lab Clin Med. 1963 Nov;62:753–761. [PubMed] [Google Scholar]
  15. SCHEIDEGGER J. J. Une micro-méthode de l'immuno-electrophorèse. Int Arch Allergy Appl Immunol. 1955;7(2):103–110. [PubMed] [Google Scholar]
  16. SCHEURLEN P. G. Uber Serumeiweissveränderungen beim Diabetes mellitus. Klin Wochenschr. 1955 Mar 1;33(9-10):198–205. doi: 10.1007/BF01467327. [DOI] [PubMed] [Google Scholar]
  17. STORMONT C., SUZUKI Y. GENETIC CONTROL OF ALBUMIN PHENOTYPES IN HORSES. Proc Soc Exp Biol Med. 1963 Dec;114:673–675. doi: 10.3181/00379727-114-28766. [DOI] [PubMed] [Google Scholar]
  18. WIEME R. J. On the presence of two albumins in certain normal human sera and its genetic determination. Clin Chim Acta. 1960 May;5:443–445. doi: 10.1016/0009-8981(60)90152-2. [DOI] [PubMed] [Google Scholar]

Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES