A familial pericentric inversion of chromosome 8 analysed with a high resolution chromosome banding technique
- 23 April 1982
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 21 (4) , 266-270
- https://doi.org/10.1111/j.1399-0004.1982.tb00761.x
Abstract
A familial pericentric inversion of chromosome 8 is described. The break points were localized by a high resolution chromosome banding technique and found to be inv(8)(p23.108q12.100). None of the family members had an unbalanced product of the inversion. There were no phenotypical abnormalities in the carriers. The break points and segregation pattern are compared with those of previously reported pericentric inversions of chromosome 8.Keywords
This publication has 8 references indexed in Scilit:
- G-banding patterns of high-resolution human chromosomes 6?22, X, and YHuman Genetics, 1979
- A fetus with recombinant of chromosome 8 inherited from her carrier fatherHuman Genetics, 1978
- Break Points in Human ChromosomesHuman Heredity, 1978
- LARGE PERICENTRIC INVERSION OF HUMAN CHROMOSOME-81976
- Familial inversion of chromosome No. 8Humangenetik, 1975
- Localization of Sister Chromatid Exchanges in Human ChromosomesScience, 1974
- An Analysis of the Break Points of Structural Rearrangements in ManJournal of Medical Genetics, 1974
- Pericentric inversion of a group C autosome: a study of three familiesAnnals of Human Genetics, 1968