Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique
- PMID: 1550115
- PMCID: PMC1682652
Analysis of reciprocal translocations by chromosome painting: applications and limitations of the technique
Abstract
Fluorescent in situ hybridization with chromosome-specific DNA libraries (chromosome painting) is an important new method for assessing chromosome rearrangements. In the research presented in this paper, two familial reciprocal translocations have been studied in the balanced and unbalanced forms, using both traditional G-banding techniques and chromosome painting. Although for each case two chromosomes were involved in the rearrangement, we found that only one chromosome library was suitable for detecting the translocation. These findings illustrate both the potential and the limitations of chromosome painting as a diagnostic tool in cytogenetics.
Similar articles
-
Recombination in a male carrier of two reciprocal translocations involving chromosomes 14, 14', 15, and 21 leading to balanced and unbalanced rearrangements in offspring.Am J Med Genet A. 2005 Apr 30;134(3):309-14. doi: 10.1002/ajmg.a.30640. Am J Med Genet A. 2005. PMID: 15732062 Review.
-
Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.J Med Genet. 1998 Jul;35(7):545-53. doi: 10.1136/jmg.35.7.545. J Med Genet. 1998. PMID: 9678698 Free PMC article.
-
[In situ ++hybridization with painting probes in the definition of reciprocal translocations].Pathologica. 1994 Feb;86(1):106-9. Pathologica. 1994. PMID: 8072796 Italian.
-
Deletion of chromosome 3 and a 3;20 reciprocal translocation demonstrated by chromosome painting.Am J Med Genet. 1995 Jan 2;55(1):27-9. doi: 10.1002/ajmg.1320550109. Am J Med Genet. 1995. PMID: 7702091
-
Prader-Willi syndrome and Robertsonian translocations involving chromosome 15.Clin Genet. 1991 Apr;39(4):294-7. doi: 10.1111/j.1399-0004.1991.tb03028.x. Clin Genet. 1991. PMID: 1817468 Review.
Cited by
-
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.Am J Hum Genet. 2005 May;76(5):877-82. doi: 10.1086/429842. Epub 2005 Mar 4. Am J Hum Genet. 2005. PMID: 15750894 Free PMC article.
-
Genetic factors in congenital diaphragmatic hernia.Am J Hum Genet. 2007 May;80(5):825-45. doi: 10.1086/513442. Epub 2007 Apr 4. Am J Hum Genet. 2007. PMID: 17436238 Free PMC article. Review.
-
Diagnosis of a complex chromosomal rearrangement using fluorescent in situ hybridisation.J Med Genet. 1996 Sep;33(9):793-4. doi: 10.1136/jmg.33.9.793. J Med Genet. 1996. PMID: 8880585 Free PMC article.
-
HeLa D98/aH-2 studied by chromosome painting and conventional cytogenetical techniques.Chromosoma. 1993 Jul;102(7):473-7. doi: 10.1007/BF00357102. Chromosoma. 1993. PMID: 7690695
-
A new strategy for cryptic telomeric translocation screening in patients with idiopathic mental retardation.J Med Genet. 1998 Mar;35(3):225-33. doi: 10.1136/jmg.35.3.225. J Med Genet. 1998. PMID: 9541108 Free PMC article.
References
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources