A fluorescence in situ hybridisation (FISH) assay for submicroscopic chromosome rearrangements involving telomers.
Main Authors: | Horsley, S, Knight, S, Regan, R, Cardy, D, Lawrie, N, Flint, J, Kearney, L |
---|---|
Format: | Journal article |
Published: |
1997
|
Similar Items
-
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres.
by: Knight, S, et al.
Published: (1997) -
Novel multiple-colour fluorescence in situ hybridisation technology for the simultaneous identification of the 24 human metaphase chromosomes on a single slide: applications in the analysis of structural chromosomal rearrangements
by: Crooks, K, et al.
Published: (1999) -
Identification of a submicroscopic familial 4p;11p translocation using multiple telomere probe FISH analysis
by: Knight, S, et al.
Published: (1997) -
The detection of submicroscopic chromosome rearrangements in children with idiopathic mental retardation and physical differences
by: Slavotinek, A, et al.
Published: (1998) -
The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.
by: Flint, J, et al.
Published: (2003)