Skip to main content
Log in

Crossing-over during human spermatogenesis visualized cytologically

  • Clinical Case Reports
  • Published:
Human Genetics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  • Baltimore Conference (1975) Second international workshop on human gene mapping. Birth Defects, vol XII, no 7. The National Foundation New York

  • Bardhan S, Singh DN, Davis K (1981) Polymorphism in chromosome 4. Clin Genet 20:44–47

    Google Scholar 

  • Craig-Holmes AP, Moore FB, Shaw MW (1975) Polymorphism of human C-band heterochromatin. II. Family studies with suggestive evidence for somatic crossing-over. Am J Hum Genet 27:179–189

    Google Scholar 

  • Engel E (1980) A new genetic concept: Uniparental disomy and its potential effect, isodisomy. Am J Med Genet 6:137–143

    Google Scholar 

  • Kirkels VGH, Hustinx WJ, Scheres JMJC (1980) Habitual abortion and translocation (22q;22q): unexpected transmission from a mother to her phenotypically normal daughter. Clin Genet 18:456–461

    Google Scholar 

  • Knight LA, Gardner A, Gallie BL (1980) Familial retinoblastoma: segregation of chromosome 13 in four families. Am J Hum Genet 32:194–201

    Google Scholar 

  • Lauritsen JG, Friedrich U (1976) Origin of extra chromosomes in trisomy 16. Clin Genet 10:156–160

    Google Scholar 

  • Licznerski G, Lindsten J (1972) Trisomy in man due to maternal nondisjunction during the first mejotic division. Hereditas 70:153–154

    Google Scholar 

  • Magenis F, Palmer CG (1976) Heritability of chromosome banding variants. In: Hook EB, Porter HI (eds) Population cytogenetics. Academic Press, New York, pp 179–188

    Google Scholar 

  • McCracken AA, Daly PA, Zolnick MR, Clark AM (1978) Twins and Q-banded chromosome polymorphisms. Hum Genet 45:253–258

    Google Scholar 

  • McKenzie WH, Lubs HA (1975) Human Q and C chromosomal variation, distribution and incidence. Cytogenet Cell Genet 14:97–115

    Google Scholar 

  • McKusick VA, Ruddle FM (1977) The status of gene map of the human chromosomes. Science 196:390–405

    Google Scholar 

  • Morton CC, Corey LA, Nance WE, Brown JA (1981) Quinacrine mustard and nucleolar organizer region heteromorphisms in twins. Acta Genet Med Gamellol 30:39–49

    Google Scholar 

  • Morten JEN, Harnden DG, Bundey S (1982) Family studies on the chromosomal location of the retinoblastoma gene (Rb-1). J Med Genet 19:120–124

    Google Scholar 

  • Palmer CG, Schwartz S, Hodes ME (1980) Transmission of balanced homologous t(22q;22q) translocation from mother to normal daughter. Clin Genet 17:418–422

    Google Scholar 

  • Rethrée M-O (1977) Syndromes involving chromosomes 4, 9 and 12. In: Yunis JJ (ed) New chromosomal syndromes. Academic Press, New York, pp 119–183

    Google Scholar 

  • Sperling K, Wiesner R (1972) A rapid technique for routine use in human and comparative cytogenetics. Hum Genet 15:349–353

    Google Scholar 

  • Sumner AT (1972) A simple technique for demonstrating centromeric heterochromatin. Exp Cell Res 75:304–306

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hansmann, I., Geisler, M. & Grimm, T. Crossing-over during human spermatogenesis visualized cytologically. Hum Genet 62, 375–377 (1982). https://doi.org/10.1007/BF00304562

Download citation

  • Received:

  • Revised:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00304562

Keywords

Navigation