Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brdicka R. Evidence for linkage between haemoglobin and chromogen loci. Folia Biol (Praha) 1966;12(4):305–306. [PubMed] [Google Scholar]
- Donahue R. P., Bias W. B., Renwick J. H., McKusick V. A. Probable assignment of the Duffy blood group locus to chromosome 1 in man. Proc Natl Acad Sci U S A. 1968 Nov;61(3):949–955. doi: 10.1073/pnas.61.3.949. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gilman J. G., Smithies O. Fetal hemoglobin variants in mice. Science. 1968 May 24;160(3830):885–886. doi: 10.1126/science.160.3830.885. [DOI] [PubMed] [Google Scholar]
- HARRIS H., ROBSON E. B. Screening test for the "atypical" and "intermediate" serum-cholinesterase types. Lancet. 1963 Aug 3;2(7301):218–221. doi: 10.1016/s0140-6736(63)90116-8. [DOI] [PubMed] [Google Scholar]
- MASSIE R. W., HARTMANN R. C. Albinism and sicklemia in a Negro family. Am J Hum Genet. 1957 Jun;9(2):127–132. [PMC free article] [PubMed] [Google Scholar]
- MORTON N. E. GENETIC STUDIES OF NORTHEASTERN BRAZIL. Cold Spring Harb Symp Quant Biol. 1964;29:69–79. doi: 10.1101/sqb.1964.029.01.012. [DOI] [PubMed] [Google Scholar]
- MORTON N. E. Sequential tests for the detection of linkage. Am J Hum Genet. 1955 Sep;7(3):277–318. [PMC free article] [PubMed] [Google Scholar]
- MORTON N. E. The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type. Am J Hum Genet. 1956 Jun;8(2):80–96. [PMC free article] [PubMed] [Google Scholar]
- Mishu M. K., Nance W. E. Further evidence for close linkage of the Hb-beta and Hb-delta loci in man. J Med Genet. 1969 Jun;6(2):190–192. doi: 10.1136/jmg.6.2.190. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NEEL J. V., SCHULL W. J., SHAPIRO H. S. Absence of linkage between the genes responsible for the sickling phenomenon, the MN blood types, and the S-agglutinogen. Am J Hum Genet. 1952 Sep;4(3):204–208. [PMC free article] [PubMed] [Google Scholar]
- NEEL J. V., SCHULL W. J., SHAPIRO H. S. Absence of linkage between the genes responsible for the sickling phenomenon, the MN blood types, and the S-agglutinogen. Am J Hum Genet. 1952 Sep;4(3):204–208. [PMC free article] [PubMed] [Google Scholar]
- Nance W. E. Genetic Control of Hemoglobin Synthesis. Science. 1963 Jul 12;141(3576):123–130. doi: 10.1126/science.141.3576.123. [DOI] [PubMed] [Google Scholar]
- PEARSON H. A., MOORE M. M. HUMAN HEMOGLOBIN GENE LINKAGE: REPORT OF A FAMILY WITH HEMOGLOBIN B2, HEMOGLOBIN S, AND BETA THALASSEMIA, INCLUDING A PROBABLE CROSSOVER BETWEEN THALASSEMIA AND DELTA LOCI. Am J Hum Genet. 1965 Mar;17:125–132. [PMC free article] [PubMed] [Google Scholar]
- POPP R. A. Studies on the mouse hemoglobin loci. II. Position of the hemoglobin locus with respect to albinism and shaker-1 loci. J Hered. 1962 Mar-Apr;53:73–80. doi: 10.1093/oxfordjournals.jhered.a107127. [DOI] [PubMed] [Google Scholar]
- Rapley S., Robson E. B., Harris H., Smith S. M. Data on the incidence, segregation and linkage relations of the adenylate kinase (AK) polymorphism. Ann Hum Genet. 1968 Jan;31(3):237–242. doi: 10.1111/j.1469-1809.1968.tb00554.x. [DOI] [PubMed] [Google Scholar]
- Renwick J. H. Progress in mapping human autosomes. Br Med Bull. 1969 Jan;25(1):65–73. doi: 10.1093/oxfordjournals.bmb.a070673. [DOI] [PubMed] [Google Scholar]
- Snyder L. H., Russell H., Graham E. B. Linkage Between the Genes for Sickle Cells and the M-N Blood Types. Science. 1947 Oct 10;106(2754):347–348. doi: 10.1126/science.106.2754.347-a. [DOI] [PubMed] [Google Scholar]
- Witkop C. J., Jr, Nance W. E., Rawls R. F., White J. G. Autosomal recessive oculocutaneous albinism in man. Evidence for genetic heterogeneity. Am J Hum Genet. 1970 Jan;22(1):55–74. [PMC free article] [PubMed] [Google Scholar]
- Ying K. L., Ives E. J. Asymmetry of chromosome number 1 pair in three generations of a phenotypically normal family. Can J Genet Cytol. 1968 Sep;10(3):575–589. doi: 10.1139/g68-076. [DOI] [PubMed] [Google Scholar]