Abstract
An azoospermic patient with an inherited inversion of chromosome 1 and a normal Y chromosome is described. The mother of the patient has the same inversion.
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- Boué J., Taillemite J. L., Hazael-Massieux P., Léonard C., Boué A. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families. Humangenetik. 1975 Sep 20;30(3):217–224. doi: 10.1007/BF00279187. [DOI] [PubMed] [Google Scholar]
- Chandley A. C. The origin of chromosomal aberrations in man and their potential for survival and reproduction in the adult human population. Ann Genet. 1981;24(1):5–11. [PubMed] [Google Scholar]
- Daniel A. Structural differences in pericentric inversions. Application to a model of risk of recombinants. Hum Genet. 1981;56(3):321–328. doi: 10.1007/BF00274687. [DOI] [PubMed] [Google Scholar]
- Dutrillaux B., Gueguen J. Etude méiotique et mitotique dans un cas de translocation t(5;Y) Humangenetik. 1975;27(3):241–245. doi: 10.1007/BF00278352. [DOI] [PubMed] [Google Scholar]
- Giraldo A., Silva E., Martínez I., Campos C., Guzmán J. Pericentric inversion of chromosome 1 in three sterile brothers. Hum Genet. 1981;58(2):226–227. doi: 10.1007/BF00278718. [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]