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. 1971 Jun;8(2):202–208. doi: 10.1136/jmg.8.2.202

A familial variant of chromosome 9.

C G Palmer, J Schroder
PMCID: PMC1469008  PMID: 5096543

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Selected References

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

  1. Bruere A. N., McLaren R. D. The idiogram of the sheep with particular reference to secondary constrictions. Can J Genet Cytol. 1967 Sep;9(3):543–553. doi: 10.1139/g67-058. [DOI] [PubMed] [Google Scholar]
  2. COHEN M. M., SHAW M. W. EFFECTS OF MITOMYCIN C ON HUMAN CHROMOSOMES. J Cell Biol. 1964 Nov;23:386–395. doi: 10.1083/jcb.23.2.386. [DOI] [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. 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]
  5. Emerit I., Vernant P. Anomalie d'un chromosome du group C chez plusiers membres d'une même famille. Humangenetik. 1968;6(4):326–334. [PubMed] [Google Scholar]
  6. JACKSON R. C. PREFERENTIAL SEGREGATION OF CHROMOSOMES FROM A TRIVALENT IN HAPLOPAPPUS GRACILIS. Science. 1964 Jul 31;145(3631):511–513. doi: 10.1126/science.145.3631.511. [DOI] [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. 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]
  9. Moores E. C., Anders J. M., Emanuel R. Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease. Ann Hum Genet. 1966 Jul;30(1):77–84. doi: 10.1111/j.1469-1809.1966.tb00008.x. [DOI] [PubMed] [Google Scholar]
  10. Nance W. E., Conneally M., Kang K. W., Reed T., Schroder J., Rose S. Genetic linkage analysis of human hemoglobin variants. Am J Hum Genet. 1970 Jul;22(4):453–459. [PMC free article] [PubMed] [Google Scholar]
  11. Palmer C. G., Funderburk S. Secondary constrictions in human chromosomes. Cytogenetics. 1965;4(4):261–276. doi: 10.1159/000129863. [DOI] [PubMed] [Google Scholar]
  12. Rhoades M. M., Dempsey E. The Effect of Abnormal Chromosome 10 on Preferential Segregation and Crossing over in Maize. Genetics. 1966 May;53(5):989–1020. doi: 10.1093/genetics/53.5.989. [DOI] [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. Sands V. E. Short arm enlargement in acrocentric chromosomes. Am J Hum Genet. 1969 May;21(3):293–304. [PMC free article] [PubMed] [Google Scholar]
  15. Schmid W., Vischer D. Spontaneous fragility of an abnormally wide secondary constriction region in a human chromosome no. 9. Humangenetik. 1969;7(1):22–27. doi: 10.1007/BF00278689. [DOI] [PubMed] [Google Scholar]
  16. 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]
  17. 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]
  18. Zimmering S. A Genetic Study of Segregation in a Translocation Heterozygote in Drosophila. Genetics. 1955 Nov;40(6):809–825. doi: 10.1093/genetics/40.6.809. [DOI] [PMC free article] [PubMed] [Google Scholar]

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