A Familial Extra Small Marker Autosome in Persons with Normal Phenotype
- 1 January 1979
- journal article
- research article
- Published by S. Karger AG in Human Heredity
- Vol. 29 (6) , 371-373
- https://doi.org/10.1159/000153075
Abstract
The propositus was referred because of sterility and oligospermia. His karyotype was 45, XY, t(13q14q). His father was dead; his mother and the only brother, who was fertile, both had 47 chromosomes, but a normal phenotype and normal intelligence. The additional chromosome was three quarters the size of a G chromosome and had satellites on the short and long arms.This publication has 3 references indexed in Scilit:
- Significance of detection of extra metacentric microchromosome in amniotic cell culture.Journal of Medical Genetics, 1978
- Autosomal reciprocal translocations and 13/14 translocations: A population studyClinical Genetics, 1976
- Partial D 15 TrisomyHuman Heredity, 1975