Skip to main content
Log in

A reply: pericentric inversion of chromosome 9qh are “real” but the mechanisms of their origin are highly complex

  • Letter to the Editor
  • 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

  • Babu KA, Verma RS (1986) Characterization of human chromosomal heterochromatin. Can J Genet Cytol 28:631–644

    CAS  PubMed  Google Scholar 

  • Conte, RA, Gupta S, Brennan JP, Verma RS (1995) Rare variants of chromosome 9 with extra G-positive bands within the qh region are not alike. J Med Genet 32:405–406

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Hoo JJ (1992) A new chromosome 9 variant: an extra band within the 9qh region. Clin Genet 41:157–158

    Article  CAS  PubMed  Google Scholar 

  • Jalal SM, Kukolish MK, Garcia M, Day DW (1990) Euchromatic 9qh+ heteromorphism in a family. Am J Med Genet 37:155–156

    Article  CAS  PubMed  Google Scholar 

  • Knight LA, Soon GM, Tan M (1993) Extra G positive band on the long arm of chromosome 9. J Med Genet 30:613

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Luke S, Verma RS, PeBenito R, Macera MJ (1991) Inversion duplication of bands q13q21 of human chromosome 9. Am J Med Genet 40:57–60

    Article  CAS  PubMed  Google Scholar 

  • Luke S, Verma RS, Conte RA, Mathews T (1992) Molecular characterization of the secondary constriction region (qh) of human chromosome 9 with pericentric inversion. J Cell Science 103: 919–923

    CAS  PubMed  Google Scholar 

  • Macera, MJ, Verma RS, Conte RA, Bialer MS, Klein VR (1995) Mechanisms of the origin of a G-positive band within the secondary constriction region of human chromosome 9. Cytogenet. Cell Genet. 69:235–239

    Article  CAS  PubMed  Google Scholar 

  • Madan K (1978) an extra band in human 9qh+ chromosome. Hum Genet 43:259–264

    Article  CAS  PubMed  Google Scholar 

  • Madan K, Bobrow M (1974) Structural variation in chromosome no. 9. Ann Genet (Paris) 17:81–86

    CAS  Google Scholar 

  • Park JP, Wojiski SA, Spellman RA, Rodes C Mohandas TK (1998) Human chromosome 9 peri centric homologies: implications for chromosome 9 heteromorphism. Cytogenet Cell Genet 82:192–194

    Article  CAS  PubMed  Google Scholar 

  • Ramesh KH, Verma RS (1996) Breakpoints in alpha, beta and satellite III DNA sequences of chromosome 9 result in a variety of pericentric inversions. J Med Genet 33:395–398

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Rivera H, Gutierrez-Angulo M, Gonzalez-Garcia JR (1999) Chromosome 9qh inversions may not be true inversions. Hum Gen DOl 1O.1007/s004399900072

    Google Scholar 

  • Reddy KS (1996) Variants of chromosome 9 with additional euchromatic bands: two case reports. Am J Med Genet 64:536–538

    Article  CAS  PubMed  Google Scholar 

  • Rocchi M, Archidiacono N, Ward DC, Baldini A (1994) A human chromosome 9-specific alphoid DNA repeat spatially resolvable from satellite 3 DNA by fluorescence in situ hybridization. Genomics 9:517–523

    Article  Google Scholar 

  • Samonte RV, Conte RA, Ramesh KH, Verma RS (1996) Molecular cytogenetic characterization of breakpoints involving pericentric inversions of human chromosome 9. Hum Genet 98: 576–580

    Article  CAS  PubMed  Google Scholar 

  • Verma RS (1988) Heterochromatin: molecular and structural aspects. Cambridge University Press, New York, pp276–292

    Google Scholar 

  • Wang JC-C, Miller WA (1994) Molecular cytogenetic characterization of two types of chromosome 9 variants. Cytogenet Cell Genet 67: 190–192

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Verma, R. A reply: pericentric inversion of chromosome 9qh are “real” but the mechanisms of their origin are highly complex. Hum Genet 105, 183–184 (1999). https://doi.org/10.1007/s004399900086

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s004399900086

Keywords

Navigation