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Mosaic ratio quantification of isochromosome 12p in Pallister-Killian syndrome using droplet digital PCR.
Fujiki, Katsunori; Shirahige, Katsuhiko; Kaur, Maninder; Deardorff, Matthew A; Conlin, Laura K; Krantz, Ian D; Izumi, Kosuke.
Afiliación
  • Fujiki K; Research Center for Epigenetic Disease, Institute for Molecular and Cellular Biosciences The University of Tokyo Tokyo Japan.
  • Shirahige K; Research Center for Epigenetic Disease, Institute for Molecular and Cellular Biosciences The University of Tokyo Tokyo Japan.
  • Kaur M; Division of Human Genetics The Children's Hospital of Philadelphia Philadelphia Pennsylvania.
  • Deardorff MA; Division of Human GeneticsThe Children's Hospital of PhiladelphiaPhiladelphiaPennsylvania; The Perelman School of Medicine at The University of PennsylvaniaPhiladelphiaPennsylvania.
  • Conlin LK; The Perelman School of Medicine at The University of PennsylvaniaPhiladelphiaPennsylvania; Department of Pathology and Laboratory MedicineThe Children's Hospital of PhiladelphiaPhiladelphiaPennsylvania19104.
  • Krantz ID; Division of Human GeneticsThe Children's Hospital of PhiladelphiaPhiladelphiaPennsylvania; The Perelman School of Medicine at The University of PennsylvaniaPhiladelphiaPennsylvania.
  • Izumi K; Research Center for Epigenetic Disease, Institute for Molecular and Cellular Biosciences The University of Tokyo Tokyo Japan.
Mol Genet Genomic Med ; 4(3): 257-61, 2016 May.
Article en En | MEDLINE | ID: mdl-27247953
BACKGROUND: Pallister-Killian syndrome (PKS) is a prototypic mosaic aneuploidy syndrome caused by mosaic supernumerary marker isochromosome 12p. Cells possessing the isochromosome 12p rapidly diminish after birth in the peripheral blood, often necessitating a skin biopsy for diagnosis. Therefore, a genomic testing that is capable of detecting low percent mosaic isochromosome 12p is preferred for the diagnosis of PKS. METHODS: The utility of the droplet digital PCR system in quantifying the mosaic ratio of isochromosome 12p in PKS was evaluated. RESULTS: Droplet digital PCR was able to precisely quantify isochromosome 12p mosaic ratio, and copy number measured by droplet digital PCR was correlated well with that of fluorescence in situ hybridization analysis. CONCLUSION: Droplet digital PCR should be considered as an effective tool for both clinical and research analytics to precisely quantify mosaic genomic copy number alterations or mosaic mutations.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Mol Genet Genomic Med Año: 2016 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Mol Genet Genomic Med Año: 2016 Tipo del documento: Article