3100 or 310 automatic capillary genetic analyzer (Thermo Fisher)
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Thermo Fisher
3100 or 310 automatic capillary genetic analyzer
3100 Or 310 Automatic Capillary Genetic Analyzer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3100+automatic+capillary+genetic+analyzer/pm36275728-74-31-31
Average 90 stars, based on 1 article reviews
3100 Or 310 Automatic Capillary Genetic Analyzer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/3100+automatic+capillary+genetic+analyzer/pm36275728-74-31-31
Average 90 stars, based on 1 article reviews
3100 or 310 automatic capillary genetic analyzer - by Bioz Stars,
2026-09
90/100 stars
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Polymerase Chain Reaction:Article Title: [Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]. Article Snippet: Három, a PWS/Angelman-régión kívül eső locus (D15S144, D15S1007 és D15S642) genotipizálása segített különbséget tenni a deletio és az uniparentalis disomia között: az apai kritikus régió hiánya és a biparentalis megjelenés a régión kívül együttesen deletiót jelentett, míg az uniparentalis öröklődés – mind a kritikus régió- ban, mind pedig azon kívül – uniparentalis disomiára utalt. .. Az MSA során a Article Title: Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Article Snippet: Is There a Higher Incidence of Maternal Uniparental Disomy 14 [upd(14)mat]?. Detection of 10 New Patients by Methylation-Specific PCR Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike Angelika Mau-Holzmann, Eva-Christina Prott, Dagmar Wieczorek, and Gabriele Gillessen-Kaesbach* Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany Institut für Humangenetik und Anthropologie, Universitätsklinikum Jena, Jena, Germany Institut für Anthropologie und Humangenetik, Universitätsklinikum Tübingen, Tübingen, Germany Institut für Humangenetik Lübeck, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany Fluorescence:Article Title: Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Article Snippet: Is There a Higher Incidence of Maternal Uniparental Disomy 14 [upd(14)mat]?. Detection of 10 New Patients by Methylation-Specific PCR Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike Angelika Mau-Holzmann, Eva-Christina Prott, Dagmar Wieczorek, and Gabriele Gillessen-Kaesbach* Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany Institut für Humangenetik und Anthropologie, Universitätsklinikum Jena, Jena, Germany Institut für Anthropologie und Humangenetik, Universitätsklinikum Tübingen, Tübingen, Germany Institut für Humangenetik Lübeck, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany Software:Article Title: Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR. Article Snippet: Is There a Higher Incidence of Maternal Uniparental Disomy 14 [upd(14)mat]?. Detection of 10 New Patients by Methylation-Specific PCR Diana Mitter, Karin Buiting, Ferdinand von Eggeling, Alma Kuechler, Thomas Liehr, Ulrike Angelika Mau-Holzmann, Eva-Christina Prott, Dagmar Wieczorek, and Gabriele Gillessen-Kaesbach* Institut für Humangenetik, Universitätsklinikum Essen, Essen, Germany Institut für Humangenetik und Anthropologie, Universitätsklinikum Jena, Jena, Germany Institut für Anthropologie und Humangenetik, Universitätsklinikum Tübingen, Tübingen, Germany Institut für Humangenetik Lübeck, Universitätsklinikum Schleswig-Holstein, Lübeck, Germany Article Title: Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Article Snippet: PCR products derived from the bisulfite-converted SNURFSNRPN promoter/exon 1 region were cloned into the pGEM-T easy vector (Promega). .. Ten clones were picked and analyzed by DNA sequencing using an ABI Clone Assay:Article Title: Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Article Snippet: PCR products derived from the bisulfite-converted SNURFSNRPN promoter/exon 1 region were cloned into the pGEM-T easy vector (Promega). .. Ten clones were picked and analyzed by DNA sequencing using an ABI DNA Sequencing:Article Title: Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Article Snippet: PCR products derived from the bisulfite-converted SNURFSNRPN promoter/exon 1 region were cloned into the pGEM-T easy vector (Promega). .. Ten clones were picked and analyzed by DNA sequencing using an ABI |