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Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization |
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| Authors: | Rina Plattner Nyla A. Heerema Patricia N. Howard-Peebles Judith H. Miles Shirley Soukup Catherine G. Palmer |
| Affiliation: | (1) Department of Medical and Molecular Genetics, Indiana University School of Medicine, 975 W. Walnut Street, 46202-5251 Indianapolis, IN, USA;(2) Genetics and IVF Institute, 3020 Javier Road, 22031 Fairfax, VA, USA;(3) Department of Human Genetics, Medical College of Virginia, Richmond, Virginia, USA;(4) Department of Medical Genetics, University of Missouri Medical Center, Columbia, MO, USA;(5) Department of Pediatrics, College of Medicine, Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH, USA |
| Abstract: | Twenty-seven patients carrying marker chromosomes were previously collected, characterized by cytogenetic techniques, and identified by stepwise fluorescence in situ hybridization (FISH) with alpha-satellite DNA probes. Clinical features of 22 patients are described here and compared to other patients with marker chromosomes similarly identified and reported in the literature. |
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