Pages that link to "Q84957131"

The following pages link to High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarrays (Q84957131):

Displaying 12 items.

• Detection of inherited mutations for breast and ovarian cancer using genomic capture and massively parallel sequencing (Q24606803) (← links)
• Single-step capture and sequencing of natural DNA for detection of BRCA1 mutations (Q30465156) (← links)
• Next-generation sequencing for cancer diagnostics: a practical perspective. (Q34238930) (← links)
• Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1. (Q35030967) (← links)
• Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes. (Q35749677) (← links)
• Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs. (Q37610127) (← links)
• Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis (Q38976987) (← links)
• Large scale mtDNA sequencing reveals sequence and functional conservation as major determinants of homoplasmic mtDNA variant distribution (Q40062641) (← links)
• The frequency of cancer predisposition gene mutations in hereditary breast and ovarian cancer patients in Taiwan: From BRCA1/2 to multi-gene panels. (Q42367527) (← links)
• A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genes (Q57970852) (← links)
• Rapid detection of gene mutations responsible for non-syndromic aortic aneurysm and dissection using two different methods: resequencing microarray technology and next-generation sequencing (Q59697638) (← links)
• Explaining cancer type specific mutations with transcriptomic and epigenomic features in normal tissues. (Q64912728) (← links)