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Furthermore, it is a common practice to screen mutation hotspots in known cancer genes, for example, the selective analysis of codons 12 and 13 in the RAS genes.
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Several issues arise when considering adding mutations to a carrier screening mutation panel.
A recent study using multi-modal screening, including whole body MRI scans, found tumors in seven of 15 screened mutation carriers.
Screening mutation analyses of genes known to be affected in other tumor types have so far revealed relatively few GCTs with mutations.
And then we screened mutations, but no mutation was detected.
Methods: We screened mutations in these genes of 25 Japanese OCA patients who lacked mutations in the OCA1 and OCA2 genes with SSCP/heteroduplexes method.
Resequencing microarrays provide a rapid and cost effective method for screening mutations in genetically heterogeneous diseases such as CMSs.
We systematically screened mutations at the promoter region, all the exons and their flanking intronic sequences of the DLG4 gene in all patients using PCR-direct autosequencing.
Sequence analysis based on custom resequencing microarrays has recently emerged as a powerful strategy for screening mutations in multiple genes linked to a common phenotype [14] [16].
Screening mutations in a conserved region or functional domain will increase the efficiency and speed for finding such deleterious mutants.
We next screened mutations in exons 5 8 of TP53 that encode the DNA binding domain and are known to harbor majority of mutations [ 9].
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