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Science 14 June 1968:
Vol. 160. no. 3833, pp. 1230 - 1231
DOI: 10.1126/science.160.3833.1230
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Articles

Haptoglobin and Catalase Loci in Man: Possible Genetic Linkage

Walter E. Nance 1, Judith E. Empson 1, Thomas W. Bennett 1, and Larry Larson 2

1 Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37203
2 University of Wisconsin Medical School, Madison 53706

Slow- and fast-migrating electrophoretic variants of human erythrocyte catalase were encountered in four of approximately 200 families. Tests for nine genetic polymorphisms provided evidence suggesting linkage only in the case of the haptoglobin system.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
TaqMan-Based Real-Time PCR for Genotyping Common Polymorphisms of Haptoglobin (HP1 and HP2).
M. Soejima and Y. Koda (2008)
Clin. Chem. 54, 1908-1913
   Abstract »    Full Text »    PDF »
Familial Deletion of the Short Arm of the D1-Chromosome (46, XX, 13 p-) Not Associated with Loss of Haptoglobin or Catalase Activity.
C. E. Parker, R. Koch, J. Mavalwala, A. Derencsenyi, and A. Hatashita (1969)
Clinical Pediatrics 8, 453-458
   Abstract »    PDF »


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Science. ISSN 0036-8075 (print), 1095-9203 (online)