Objective: To delineate the chromosome structural aberration in a case of chromosome translocation by fluorescence in situ hybridization (FISH) technique and precisely identify the breakpoints. Methods: The whole chromosome point 5(wcp5) and locus-specific probes derived from yeast artificial chromosomes (YACs) mapping the nearby region of breakpoints were used to delineate the translocation t(5;10) found by high resolution G-banding examination in a case with congenital abnormality. Results: A balanced translocation was confirmed and the breakpoints were located in the 1. 5 Mb area on chromosome 5 and within the approximately 3 Mb interval on chromosome 10. Conclusion: The phenotypic abnormality might result from the disruption of disease-associated gene(s) or microrearrangement(s) on the site of breakpoint(s).
|Zeitschrift||Chinese Journal of Medical Genetics|
|Seiten (von - bis)||96-99|
|Publikationsstatus||Veröffentlicht - 2001|
Strategische Forschungsbereiche und Zentren
- Querschnittsbereich: Medizinische Genetik