Marker chromosome identification by micro-FISH
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1996.tb03781.x/fullpdf
Reference34 articles.
1. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization;Blennow;Am J Med Genet,1995
2. Forty-four probands with an additional “marker” chromosome;Buckton;Hum Genet,1985
3. The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization;Callen;Am J Hum Genet,1990
4. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes;Callen;Am J Med Genet,1992
5. Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics;Carter;J Med Genet,1992
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1. Prenatal identification of de novo marker chromosomes using micro-FISH approach;Clinical Genetics;2008-06-28
2. Reverse chromosome painting for the identification of marker chromosomes and complex translocations in leukemia;Cytometry;1999-02-01
3. Detection of structural chromosome damage in rat interphase cells using region-specific fluorescence in situ hybridization probes developed by microdissection;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;1998-11
4. Characterization of a de novo unbalanced translocation t(14q18q) using microdissection and fluorescence in situ hybridization;American Journal of Medical Genetics;1998-02-03
5. Characterization of marker chromosomes by fish using microdissected probes from old carnoy-fixed cells: Report of two cases;Japanese Journal of Human Genetics;1997-12
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