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Volumn 50, Issue 1, 2004, Pages 203-206

Multiplex Single-Nucleotide Primer Extension Analysis to Simultaneously Detect Eleven BRCA1 Mutations in Breast Cancer Families

Author keywords

[No Author keywords available]

Indexed keywords

ANALYTIC METHOD; ARTICLE; BREAST CANCER; DIAGNOSTIC ACCURACY; DNA DETERMINATION; DNA EXTRACTION; EXON; FEMALE; GENE MUTATION; HUMAN; MULTIPLEX SINGLE NUCLEOTIDE PRIMER EXTENSION ANALYSIS; ONCOGENE; OVARY CANCER; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 1642492773     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1373/clinchem.2003.023713     Document Type: Article
Times cited : (7)

References (10)
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    • (1995) JAMA , vol.273 , pp. 535-541
    • Shattuck-Eidens, D.1    McClure, M.2    Simard, J.3    Labrie, F.4    Narod, S.5    Couch, F.6
  • 3
    • 84876083286 scopus 로고    scopus 로고
    • Breast Cancer Information Core. http://www.nhgri.nih.gov/Intramural_ research/Lab_transfer/Bic/ (Accessed January 2003).
    • Breast Cancer Information Core
  • 4
    • 16944364123 scopus 로고    scopus 로고
    • BRCA1 sequence variations in 160 individuals referred to a breast/ ovarian family cancer clinic
    • Institut Curie Breast Cancer Group
    • Stoppa-Lyonnet D, Laurent-Puig P, Essioux L, Pages S, Ithier G, Ligot L, et al. BRCA1 sequence variations in 160 individuals referred to a breast/ ovarian family cancer clinic. Institut Curie Breast Cancer Group. Am J Hum Genet 1997;60:1021-30.
    • (1997) Am J Hum Genet , vol.60 , pp. 1021-1030
    • Stoppa-Lyonnet, D.1    Laurent-Puig, P.2    Essioux, L.3    Pages, S.4    Ithier, G.5    Ligot, L.6
  • 5
    • 0031678853 scopus 로고    scopus 로고
    • New mechanism of BRCA-1 mutation by deletion/insertion at the same nucleotide position in three unrelated French breast/ ovarian cancer families
    • Presneau N, Laplace-Marieze V, Sylvain V, Hardouin A, Bernard-Gallon D, Bignon YJ. New mechanism of BRCA-1 mutation by deletion/insertion at the same nucleotide position In three unrelated French breast/ ovarian cancer families. Hum Genet 1998;103:334-9.
    • (1998) Hum Genet , vol.103 , pp. 334-339
    • Presneau, N.1    Laplace-Marieze, V.2    Sylvain, V.3    Hardouin, A.4    Bernard-Gallon, D.5    Bignon, Y.J.6
  • 6
    • 16944365091 scopus 로고    scopus 로고
    • A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgium hereditary breast and ovarian cancer families
    • Peelen T, van Vliet M, Petrij-Bosch A, Mieremet R, Szabo C, van den Ouweland A, et al. A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgium hereditary breast and ovarian cancer families. Am J Human Genet 1997;60:1041-9.
    • (1997) Am J Human Genet , vol.60 , pp. 1041-1049
    • Peelen, T.1    Van Vliet, M.2    Petrij-Bosch, A.3    Mieremet, R.4    Szabo, C.5    Van Den Ouweland, A.6
  • 8
    • 0031882769 scopus 로고    scopus 로고
    • Germline BRCA1 mutations in patients from 84 families with breast and/or ovarian cancers in northern France
    • Peyrat JP, Vennin P, Hornez L, Fournier J, Adenis C, Bonneterre J. Germline BRCA1 mutations In patients from 84 families with breast and/or ovarian cancers in northern France. Eur J Cancer Prev 1998;7:S7-12.
    • (1998) Eur J Cancer Prev , vol.7
    • Peyrat, J.P.1    Vennin, P.2    Hornez, L.3    Fournier, J.4    Adenis, C.5    Bonneterre, J.6
  • 10
    • 0036274380 scopus 로고    scopus 로고
    • Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia
    • Krone N, Braun A, Weinert S, Peter M, Roscher AA, Partsch CJ, et al. Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasia. Clin Chem 2002;48:818-25.
    • (2002) Clin Chem , vol.48 , pp. 818-825
    • Krone, N.1    Braun, A.2    Weinert, S.3    Peter, M.4    Roscher, A.A.5    Partsch, C.J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.