follicular-unit 发表于 2025-3-23 09:45:19
Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms Conferring Risk of Myocarght result from the interactions of multiple genetic and environmental factors, none of which can cause disease solely by themselves. To reveal the genetic bases of MI, we performed a large-scale, case-control association study using 92,788 gene-based single-nucleotide polymorphism (SNP) markers. WePAN 发表于 2025-3-23 16:44:21
Mutation Detection in Congenital Long QT Syndrome,arrhythmogenic disorders such as long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT), Andersen-Tawil syndrome, Brugada Syndrome, and Timothy syndrome. In addition, the genetic basis for cardiomyopathic processes vulnerable to sudden arrhythmic death—hypertrophic carInferior 发表于 2025-3-23 19:25:41
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https://doi.org/10.1007/978-3-642-24226-7ns, and other complicated chromosomal changes. Fluorescence . hybridization (FISH), a technique involving hybridization of labeled probes to chromosomes and detection of hybridization via fluorochromes, has become a popular method for identification and characterization of cytogenetic abnormalities.Condyle 发表于 2025-3-24 13:56:03
https://doi.org/10.1007/978-3-642-24226-7complex clinical phenotypes. Comparative genomic hybridization by microarray (array CGH) is a high-throughput and high-resolution method for the detection of microscopic and submicroscopic chromosome abnormalities, some of which may not be detectable by conventional cytogenetic techniques. In additi带来墨水 发表于 2025-3-24 15:58:40
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