A retrospective CISS hybridization analysis of a case with de novo translocation t(18;22) resulting in an 18p-syndrome*
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03827.x/fullpdf
Reference7 articles.
1. A fluorescence in situ hybridization technique for retrospective cytosenetic analysis;Babu;Cytogenet Cell Genet,1991
2. 18p-syndrome with a single central maxillary incisor;Dolan;J Med Genet,1981
3. Graves disease in a patient with the del(18p) syndrome;Jones;Am J Med Genet,1982
4. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries;Lichter;Hum Genet,1988
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1. De novo isochromosome 18p in two patients: cytogenetic diagnosis and confirmation by chromosome painting;Clinical Genetics;2008-06-28
2. Single mandibular incisor in a patient with del (18p) anomaly;Clinical Genetics;2008-04-23
3. Basilar artery dolichoectasia in a boy with a combination of partial monosomy 18p and partial trisomy 20q;Clinical Dysmorphology;2006-10
4. Subtelomeric deletion of 18p in an adult with paranoid schizophrenia and mental retardation;American Journal of Medical Genetics;2003
5. Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangements.;Journal of Medical Genetics;1998-09-01
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