Abstract
A pericentric inv(11)(p12q25) was detected by prenatal diagnosis and subsequently found in four other family members. There was no apparent evidence of clinical consequences caused by this inversion.
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.
- Autio-Harmainen H., De La Chapelle A. High resolution of a small pericentric inversion of chromosome 11. J Med Genet. 1980 Feb;17(1):44–47. doi: 10.1136/jmg.17.1.44. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boué J., Boué A. Prenatal diagnosis in 100 structural rearrangements of the chromosomes. Cytogenet Cell Genet. 1978;20(1-6):213–225. doi: 10.1159/000130853. [DOI] [PubMed] [Google Scholar]
- Moorhead P. S. A closer look at chromosomal inversions. Am J Hum Genet. 1976 May;28(3):294–296. [PMC free article] [PubMed] [Google Scholar]
- Mutton D. E., Daker M. G. Pericentric inversion of chromosome 9. Nat New Biol. 1973 Jan 17;241(107):80–80. doi: 10.1038/newbio241080a0. [DOI] [PubMed] [Google Scholar]
- Simola K., Karli P., De La Chapelle A. Two pericentric inversions of human chromosome 11. J Med Genet. 1977 Oct;14(5):371–374. doi: 10.1136/jmg.14.5.371. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sutherland G. R., Gardiner A. J., Carter R. F. Familial pericentric inversion of chromosome 19, inv(19) (p13q13) with a note on genetic counseling of pericentric inversion carriers. Clin Genet. 1976 Jul;10(1):54–59. doi: 10.1111/j.1399-0004.1976.tb00009.x. [DOI] [PubMed] [Google Scholar]
- Winsor E. J., Palmer C. G., Ellis P. M., Hunter J. L., Ferguson-Smith M. A. Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7. Cytogenet Cell Genet. 1978;20(1-6):169–184. doi: 10.1159/000130849. [DOI] [PubMed] [Google Scholar]
- de la Chapelle A., Schröder J., Stenstrand K., Fellman J., Herva R., Saarni M., Anttolainen I., Tallila I., Tervilä L., Husa L. Pericentric inversions of human chromosomes 9 and 10. Am J Hum Genet. 1974 Nov;26(6):746–766. [PMC free article] [PubMed] [Google Scholar]