Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1968 Nov;61(3):949–955. doi: 10.1073/pnas.61.3.949

Probable assignment of the Duffy blood group locus to chromosome 1 in man.

R P Donahue, W B Bias, J H Renwick, V A McKusick
PMCID: PMC305420  PMID: 5246559

Full text

PDF

Images in this article

Selected References

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

  1. Bias W. B., Migeon B. R. Haptoglobin: a locus on the D1 chromosome? Am J Hum Genet. 1967 May;19(3 Pt 2):393–398. [PMC free article] [PubMed] [Google Scholar]
  2. CHOWN B., LEWIS M., KAITA H. THE DUFFY BLOOD GROUP SYSTEM IN CAUCASIANS: EVIDENCE FOR A NEW ALLELE. Am J Hum Genet. 1965 Sep;17:384–389. [PMC free article] [PubMed] [Google Scholar]
  3. COOPER H. L., HERNITS R. A FAMILIAL CHROMOSOME VARIANT IN A SUBJECT WITH ANOMALOUS SEX DIFFERENTIATION. Am J Hum Genet. 1963 Dec;15:465–475. [PMC free article] [PubMed] [Google Scholar]
  4. Crawford M. N., Punnett H. H., Carpenter G. G. Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage. Nature. 1967 Sep 2;215(5105):1075–1076. doi: 10.1038/2151075a0. [DOI] [PubMed] [Google Scholar]
  5. FERGUSON-SMITH M. A., FERGUSON-SMITH M. E., ELLIS P. M., DICKSON M. The sites and relative frequencies of secondary constrictions in human somatic chromosomes. Cytogenetics. 1962;1:325–343. doi: 10.1159/000129743. [DOI] [PubMed] [Google Scholar]
  6. Genest P., Mortezai M. A., Tremblay M. Le syndrome d'Apert (acrocéphalo-syndactylie). Une observation avec un chromosome 1 anormal. Arch Fr Pediatr. 1966 Oct;23(8):887–897. [PubMed] [Google Scholar]
  7. KABACK M. M., SAKSELA E., MELLMAN W. J. THE EFFECT OF 5-BROMODEOXYURIDINE ON HUMAN CHROMOSOMES. Exp Cell Res. 1964 Mar;34:182–186. doi: 10.1016/0014-4827(64)90193-4. [DOI] [PubMed] [Google Scholar]
  8. LELE K. P., DENT T., DELHANTY J. D. CHROMOSOME STUDIES IN FIVE CASES OF COLOBOMA OF THE IRIS. Lancet. 1965 Mar 13;1(7385):576–578. doi: 10.1016/s0140-6736(65)91148-7. [DOI] [PubMed] [Google Scholar]
  9. PATAU K., THERMAN E., INHORN S. L., SMITH D. W., RUESS A. L. Partial-trisomy syndromes. II. An insertion as cause of the OFD syndrome in mother and daughter. Chromosoma. 1961;12:573–584. doi: 10.1007/BF00328943. [DOI] [PubMed] [Google Scholar]
  10. Philip J., Frydenberg O., Sele V. Enlarged chromosome No. 1 in a patient with primary amenorrhoea. Cytogenetics. 1965;4(6):329–339. doi: 10.1159/000129870. [DOI] [PubMed] [Google Scholar]
  11. RENWICK J. H., LAWLER S. D. PROBABLE LINKAGE BETWEEN A CONGENITAL CATARACT LOCUS AND THE DUFFY BLOOD GROUP LOCUS. Ann Hum Genet. 1963 Aug;27:67–84. doi: 10.1111/j.1469-1809.1963.tb00782.x. [DOI] [PubMed] [Google Scholar]
  12. RENWICK J. H., SCHULZE J. AN ANALYSIS OF SOME DATA ON THE LINKAGE BETWEEN XG AND COLORBLINDNESS IN MAN. Am J Hum Genet. 1964 Dec;16:410–418. [PMC free article] [PubMed] [Google Scholar]
  13. SAKSELA E., MOORHEAD P. S. Enhancement of secondary constrictions and the heterochromatic X in human cells. Cytogenetics. 1962;1:225–244. doi: 10.1159/000129733. [DOI] [PubMed] [Google Scholar]
  14. Sofuni T., Sandberg A. A. Chronology and pattern of human chromosome replication. VI. Further studies including autoradiographic behavior of normal and abnormal no. 1 autosomes. Cytogenetics. 1967;6(5):357–370. [PubMed] [Google Scholar]
  15. Steinberg A. G., Wilson J. A. Studies on Hereditary Gamma Globulin Factors: Evidence that Gm (b) in Whites and Negroes is not the Same and that Gm-like is Determined by an Allele at the Gm Locus. Am J Hum Genet. 1963 Mar;15(1):96–105. [PMC free article] [PubMed] [Google Scholar]
  16. UCHIDA I. A., MCRAE K. N., RAY M. FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA. Am J Hum Genet. 1965 Sep;17:410–419. [PMC free article] [PubMed] [Google Scholar]
  17. YUNIS J. J., GORLIN R. J. Chromosomal study in patients with cysts of the jaw, multiple nevoid basal cell carcinomata and bifid rib syndrome. Chromosoma. 1963;14:146–153. doi: 10.1007/BF00336756. [DOI] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES