FIELD: medicine.
SUBSTANCE: oncologic mutations, associated with hereditary breast cancer are detected by determination of complete nucleotide sequence of coding part of BRCA1 gene. Amplification of coding part of BRCA1 gene by means of 28 pairs of synthetic oligonucleotides is performed with further sequencing amplification products.
EFFECT: invention makes it possible to detect mutations, associated with hereditary forms of breast cancer, with high accuracy and reliability.
1 dwg, 5 tbl, 1 ex
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Authors
Dates
2012-01-20—Published
2010-06-07—Filed