Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy
- PMID: 2879921
- PMCID: PMC1049828
- DOI: 10.1136/jmg.23.6.491
Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy
Abstract
A number of DNA probes from the short arm of the X chromosome have been used to study the inheritance of the translocation chromosomes in a girl with an X; autosome translocation and muscular dystrophy. The two translocation chromosomes were found to be derived from the father's single normal X chromosome, ruling out maternal inheritance of a pre-existent mutation and enhancing the concept that the de novo translocation is responsible for the dystrophic phenotype.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical