Cytogenetic and Genome Research · 2001 · 52 citations · 20 references
Life SciencesGeneticsMolecular GeneticsCell DivisionCytogeneticsGenomicsChromosomal AbnormalitiesComparative CytogeneticsComparative Genomic HybridizationMolecular CytogeneticsStructural Chromosome AbnormalitiesTelomere BiologyCentromere AbnormalitiesChromosome Marker IdentificationMetaphase CytogeneticsNeocentromere FormationSmall Supernumerary Marker ChromosomesTelomere AbnormalitiesTelomeric Dna Repeat Sequences
A two year-old child presented with mild developmental delay. On karyotype analysis, a supernumerary small marker chromosome (SMC) was found in all cells examined. This SMC was approximately the size of an isochromosome 18p, being symmetrical with a central constriction. C-banding and silver staining were negative and FISH with all chromosome-specific paints, centromere probes and telomere probes showed no hybridization to the SMC; telomere repeat sequences were however present on both arms. Comparative genomic hybridization showed no amplification of any chromosome region. Flow sorting of the SMC and reverse painting onto normal metaphase spreads showed no hybridization to any chromosome, whereas reverse painting onto the patient's own metaphases showed hybridization to the SMC only. This SMC may thus represent either a complex amplicon of different genomic regions, or a multifold amplification of a very small region, with a neocentromere comprising an active kinetochore but no alphoid DNA. Prognostic implications for the proband were difficult to assess due to the absence of reports of similar marker chromosomes in the literature.
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A complete set of human telomeric probes and their clinical application
Yi Ning, Anna V. Roschke, Ann C. M. Smith et al. · Nature Genetics · 1996 · 302 citations
Samantha J.L. Knight, Sharon W. Horsley, Regina Regan et al. · PubMed · 1997 · 183 citations