[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]
[Article in
Russian]
- PMID: 8721845
Item in Clipboard
[An analysis of human marker chromosomes originating from chromosome 21 by using in situ hybridization]
[Article in
Russian]
Tsitol Genet.
1995 Sep-Oct.
Abstract
Four cases of patients with additional marker chromosomes are described. The clinical, cytogenetic and molecular cytogenetic methods have been used for investigation. The identification of marker chromosomes was made by using in situ hybridization and the collection of chromosome-specific DNA probes. All marker chromosomes were determined as originated from chromosome 21 with break-points in the region between 21q11 and 21q22.
Similar articles
-
Identification of marker chromosomes by in situ hybridization technique using alpha and "classical" satellite DNA probes with relative chromosomal specificity.Tsitol Genet. 1994 May-Jun;28(3):67-70. Tsitol Genet. 1994. PMID: 7974787
-
Application of fluorescence in situ hybridization to the identification of different marker chromosomes.Ann Genet. 1998;41(1):5-10. Ann Genet. 1998. PMID: 9599644
-
[Non-radioactive in situ hybridization of alpha-satellite sequences in cytogenetic diagnosis].Pathologica. 1992 May-Jun;84(1091):363-9. Pathologica. 1992. PMID: 1465321 Italian.
-
Molecular cytogenetic study of supernumerary marker chromosomes in an unselected group of children.Am J Med Genet. 1995 Mar 13;56(1):106-11. doi: 10.1002/ajmg.1320560124. Am J Med Genet. 1995. PMID: 7747772 Review.
-
[A review of the data from cytogenetic and molecular cytogenetic research on human supernumerary minichromosomes].Tsitol Genet. 1994 Sep-Oct;28(5):81-8. Tsitol Genet. 1994. PMID: 7900203 Review. Russian.