Skip to main content
PMC home page
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1969 Sep;21(5):423–429.

Genetic linkage studies in a Negro kindred with Norrie's disease.

W E Nance, S Hara, A Hansen, J Elliott, M Lewis, B Chown
PMCID: PMC1706563  PMID: 5307229

Full text

PDF
427

Selected References

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

  1. Adam A., Tippett P., Gavin J., Noades J., Sanger R., Race R. R. The linkage relation of Xg to g-6-pd in Israelis: the evidence of a second series of families. Ann Hum Genet. 1967 Jan;30(3):211–218. doi: 10.1111/j.1469-1809.1967.tb00022.x. [DOI] [PubMed] [Google Scholar]
  2. BEARN A. G., BOWMAN B. H., KITCHIN F. D. GENETIC AND BIOCHEMICAL CONSIDERATIONS OF THE SERUM GROUP-SPECIFIC COMPONENT. Cold Spring Harb Symp Quant Biol. 1964;29:435–442. doi: 10.1101/sqb.1964.029.01.045. [DOI] [PubMed] [Google Scholar]
  3. Davidson R. G. Electrophoretic variants of human 6-phosphogluconate dehydrogenase: population and family studies and description of a new variant. Ann Hum Genet. 1967 May;30(4):355–361. doi: 10.1111/j.1469-1809.1967.tb00037.x. [DOI] [PubMed] [Google Scholar]
  4. GUTTMACHER A. F. The incidence of multiple births in man and some of the other unipara. Obstet Gynecol. 1953 Jul;2(1):22–35. [PubMed] [Google Scholar]
  5. Hansen A. C. Norrie's disease. Am J Ophthalmol. 1968 Aug;66(2):328–332. doi: 10.1016/0002-9394(68)92083-7. [DOI] [PubMed] [Google Scholar]
  6. MOORE R. E. Distribution of blood factors, ABO, MN and Rh in a group of American Negroes. Am J Phys Anthropol. 1955 Mar;13(1):121–128. doi: 10.1002/ajpa.1330130109. [DOI] [PubMed] [Google Scholar]
  7. 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]
  8. POLLITZER W. S. The Henshaw blood factor in New York City Negroes. Am J Phys Anthropol. 1956 Sep;14(3):445–447. doi: 10.1002/ajpa.1330140319. [DOI] [PubMed] [Google Scholar]
  9. Shreffler D. C., Brewer G. J., Gall J. C., Honeyman M. S. Electrophoretic variation in human serum ceruloplasmin: a new genetic polymorphism. Biochem Genet. 1967 Sep;1(2):101–115. doi: 10.1007/BF00486512. [DOI] [PubMed] [Google Scholar]
  10. Siniscalco M., Filippi G., Latte B., Piomelli S., Rattazzi M., Gavin J., Sanger R., Race R. R. Failure to detect linkage between Xg and other X-borne loci in Sardinians. Ann Hum Genet. 1966 Mar;29(3):231–252. doi: 10.1111/j.1469-1809.1966.tb00518.x. [DOI] [PubMed] [Google Scholar]
  11. Vesell E. S. Genetic control of isozyme patterns in human tissues. Prog Med Genet. 1965;4:128–175. [PubMed] [Google Scholar]
  12. WARBURG M., HAUGE M., SANGER R. NORRIE'S DISEASE AND THE XG BLOOD GROUP SYSTEM: LINKAGE DATA. Acta Genet Stat Med. 1965;15:103–115. doi: 10.1159/000151898. [DOI] [PubMed] [Google Scholar]
  13. WARBURG M. Norie's disease (atrofia bulborum hereditaria). Acta Ophthalmol (Copenh) 1963;41:134–146. doi: 10.1111/j.1755-3768.1963.tb03533.x. [DOI] [PubMed] [Google Scholar]
  14. Warburg M. Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration. Acta Ophthalmol (Copenh) 1966;(Suppl):1–47. [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES