CLINICAL SIGNIFICANCE OF THE SATELLITED SHORT ARM OF HUMAN-CHROMOSOME 17 (17PS +) - RARE HETEROMORPHISM
- 1 January 1979
- journal article
- research article
- Vol. 22 (3), 133-136
Abstract
A 43 yr old impotent male Caucasian had a chromosomal constitution of 46,XY,17ps+. The satellited chromosome 17 was also present in his sister. There is no evidence that this satellited chromosome causes any clinical abnormality. Multiple banding techniques showed that the 17ps+ is a rare chromosomal heteromorphism.This publication has 8 references indexed in Scilit:
- Familial occurrence of chromosome variant 17ph+Clinical Genetics, 2008
- Silver staining studies on the short arm variant of human chromosome 17Human Genetics, 1978
- An improved method for photographing fluorescent human chromosomes*Journal of Microscopy, 1976
- Y-chromosomal genes in a phenotypic male with a 46XX karyotypeJAMA, 1976
- ADDITIONAL OBSERVATIONS ON THE PREPARATION OF R BANDED HUMAN CHROMOSOMES WITH ACRIDINE ORANGECanadian Journal of Genetics and Cytology, 1976
- An improved technique for selective silver staining of nucleolar organizer regions in human chromosomesHuman Genetics, 1976
- THE CRI-DU-CHAT SYNDROME WITH AN APPARENTLY NORMAL KARYOTYPEThe Lancet, 1967
- Inheritance of marker chromosomes from a cytogenetic survey of congenital heart diseaseAnnals of Human Genetics, 1966