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[1]_Andrulis IL, Anton-Culver H, Beck J et al. (2002)Comparison of DNA-and RNA-based methods for detection of truncating BRCA1 mutations. Hum Mutat 20: 65–73.
[2]_Arnold N, Gross E, Schwarz-Boeger U, Pfisterer J, Jonat W, Kiechle M. (1999) A highly sensitive, fast, and economical technique for mutation analysis in hereditary breast and ovarian cancers. Hum Mutat 14:333–339.
[3]_Casadei S, Cortesi L, Pensotti V et al. (2001) Detection of germline BRCA1 mutations by Multiple-Dye Cleavase Fragment Length Polymorphism (MD-CFLP) method. Br J Cancer 85: 845–849.
[4]_Eng C, Brody LC, Wagner TM et al. (2001) Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1. J Med Genet 38: 824–833.
[5]_Ganguly T, Dhulipala R, Godmilow L, Ganguly A. (1998) High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high-risk BRCA1-negative breast cancer families. Hum Genet 102:549–556.
[6]_Gross E, Arnold N, Goette J, Schwarz-Boeger U, Kiechle M. (1999) A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC. Hum Genet 105: 72–78.
[7]_Jakubowska A, Gorski B, Byrski T et al. (2001) Detection of germline mutations in the BRCA1 gene by RNA-based sequencing. Hum Mutat 18: 149–156.
[8]_Kringen P, Egedal S, Pedersen JC et al. (2002) BRCA1 mutation screening using restriction endonuclease fingerprinting-single-strand conformation polymorphism in an automated capillary electrophoresis system. Electrophoresis 23: 4085–4091.
[9]_Rothfuss A, Schutz P, Bochum S et al. (2000) Induced micronucleus frequencies in peripheral lymphocytes as a screening test for carriers of a BRCA1 mutation in breast cancer families. [see comment]. Cancer Res. 60: 390–394.
[10]_Sakayori M, Kawahara M, Shiraishi K et al. (2003) Evaluation of the diagnostic accuracy of the stop codon (SC) assay for identifying protein-truncating mutations in the BRCA1and BRCA2genes in familial breast cancer. J Hum Genet 48: 130–137.
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Schleberger, H., Gadzicki, D., Schlegelberger, B., Gerhardus, A. (2005). Systematischer Vergleich der Testverfahren. In: Gerhardus, A., Schleberger, H., Schlegelberger, B., Schwartz, F.W. (eds) BRCA — Erblicher Brust- und Eierstockkrebs. Springer, Berlin, Heidelberg. https://doi.org/10.1007/3-540-26553-8_3
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