Related Experiment Videos
Molecular characterization of 18p deletions: evidence for a breakpoint cluster
Rebecca L Schaub1, Xavier T Reveles, Jacques Baillargeon
1Department of Pediatrics, University of Texas Health Science Center, San Antonio, Texas 78229-7809, USA.
Purpose:
To determine the size and parental origin of the deletion in individuals with 18p- syndrome.
Methods:
Molecular and fluorescence in situ hybridization analyses of the pericentromeric region of chromosome 18 were performed on genomic DNA and chromosomes from study participants.
Results:
The majority of the breakpoints were located between markers D18S852 on 18p and D18S1149 on 18q, a distance of approximately 4 Mb. The parental origin of these deletions appears to be equally distributed, half maternally derived and half paternally derived.
Conclusion:
The distributions of both the size and parental origin of the 18p deletions support the presence of a breakpoint cluster in the 18p- syndrome.