Literature DB >> 15004455

The application of region-specific probes for the resolution of duplication 8p: a case report and a review of the literature.

B Pabst1, M Arslan-Kirchner, J Schmidtke, K Miller.   

Abstract

The structural rearrangement in the short arm of a chromosome 8 in a clinically affected patient has been reinvestigated by FISH using whole chromosome painting and region specific YAC probes. An inverted duplication of the segment p22-->p11.2 and a deletion of the subtelomeric region were demonstrated. By this approach, a more detailed resolution of the duplication/deletion 8p was possible. With the application of molecular cytogenetic methods the existence of different duplication segments within the clinical entity of duplication/deficiency 8p can be shown.

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Year:  2003        PMID: 15004455     DOI: 10.1159/000076280

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  3 in total

1.  A potential relationship among beta-defensins haplotype, SOX7 duplication and cardiac defects.

Authors:  Fei Long; Xike Wang; Shaohai Fang; Yuejuan Xu; Kun Sun; Sun Chen; Rang Xu
Journal:  PLoS One       Date:  2013-08-29       Impact factor: 3.240

2.  Genomic profile of copy number variants on the short arm of human chromosome 8.

Authors:  Shihui Yu; Stephanie Fiedler; Andrew Stegner; William D Graf
Journal:  Eur J Hum Genet       Date:  2010-05-12       Impact factor: 4.246

3.  Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report.

Authors:  Dilek Aktas; Anja Weise; Eda Utine; Dursun Alehan; Kristin Mrasek; Ferdinand von Eggeling; Heike Thieme; Ergul Tuncbilek; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2009-06-30       Impact factor: 2.009

  3 in total

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