Crossref
journal-article
Springer Science and Business Media LLC
Nature Genetics (297)
References
30
Referenced
387
-
Hall, J. et al. Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250, 1684–1689 (1990).
(
10.1126/science.2270482
) / Science by J Hall (1990) -
Narod, S. et al. Familial breast-ovarian cancer locus on chromosome 17q12–q23. Lancet 338, 82–83 (1991).
(
10.1016/0140-6736(91)90076-2
) / Lancet by S Narod (1991) - Easton, D.F. et al. Genetic analysis in familial breast and ovarian cancer. Results from 214 families. Am. J. Hum. Genet. 52, 678–701 (1993). / Am. J. Hum. Genet. by DF Easton (1993)
- Rowell, S., Newman, B., Boyd, J. & King, M.C. Inherited predisposition to breast and ovarian cancer. Am. J. Hum. Genet. 55, 861–865 (1994). / Am. J. Hum. Genet. by S Rowell (1994)
-
Ford, D. and the Breast Cancer Linkage Consortium. Risks of cancer in BRCA1 -mutation carriers. Lancet 343, 692–695 (1994).
(
10.1016/S0140-6736(94)91578-4
) / Lancet by D Ford (1994) -
Miki, Y. et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1 . Science 266, 66–71 (1994).
(
10.1126/science.7545954
) / Science by Y Miki (1994) -
Shattuck-Eidens, D. et al. A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening. J. Am. Med. Assoc. 273, 535–541 (1995).
(
10.1001/jama.1995.03520310033026
) / J. Am. Med. Assoc. by D Shattuck-Eidens (1995) - A comprehensive listing of BRCA1 mutations and mutation screening protocols can be found in the Breast Cancer Information Core Database located on the World Wide Web at http://www.nchgr.nih.gov/lntramural_ research/Lab_transfer/Bic/.
-
Struewing, J.P. et al. Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including one family with male breast cancer. Am J. Hum. Genet. 57, 1–7 (1995).
(
10.1002/ajmg.1320570102
) / Am J. Hum. Genet. by JP Struewing (1995) -
Struewing, J.P. et al. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nature Genet. 11, 198–200 (1995).
(
10.1038/ng1095-198
) / Nature Genet. by JP Struewing (1995) - Tonin, P. et al. BRCA1 mutations in Ashkenazi Jewish women. Am. J. Hum. Genet. 57, 189 (1995). / Am. J. Hum. Genet. by P Tonin (1995)
- Friedman, L.S. et al. Novel inherited mutations and expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families. Am. J. Hum. Genet. 57, 1284–1297 (1995). / Am. J. Hum. Genet. by LS Friedman (1995)
-
FitzGerald, M.G. et al. Germ-line BRCA1 mutations in Jewish and non-Jewish women with early-onset breast cancer. N. Engl. J. Med. 334, 143–149 (1996).
(
10.1056/NEJM199601183340302
) / N. Engl. J. Med. by MG FitzGerald (1996) -
Offit, K. et al. Germline BRCA1 185delAG mutations in Jewish women with breast cancer. Lancet 347, 1643–1645 (1996).
(
10.1016/S0140-6736(96)91484-1
) / Lancet by K Offit (1996) -
Castilla, L.H. et al. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. Nature Genet. 8, 387–391 (1994).
(
10.1038/ng1294-387
) / Nature Genet. by LH Castilla (1994) -
Friedman, L.S. et al. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nature Genet. 8, 399–404 (1994).
(
10.1038/ng1294-399
) / Nature Genet. by LS Friedman (1994) -
Simard, J. et al. Common origins of BRCA1 in Canadian breast and ovarian cancer families. Nature Genet. 8, 392–398 (1994).
(
10.1038/ng1294-392
) / Nature Genet. by J Simard (1994) -
Hogervorst, F.B.L. et at. Rapid detection of BRCA1 mutations by the protein truncation test. Nature Genet. 10, 208–212 (1995).
(
10.1038/ng0695-208
) / Nature Genet. by FBL Hogervorst (1995) - Gayther, S.A. et al. Rapid detection of regionally clustered germ-line BRCA1 mutations by multiplex heteroduplex analysis. Am. J. Hum. Genet. 58, 451–456 (1996). / Am. J. Hum. Genet. by SA Gayther (1996)
-
Gayther, S.A. et al. Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype-phenotype correlation. Nature Genet. 11, 428–433 (1995).
(
10.1038/ng1295-428
) / Nature Genet. by SA Gayther (1995) -
Fodor, S.P.A. et al. Light-directed spatially addressable parallel chemical synthesis. Science 251, 767–773 (1991).
(
10.1126/science.1990438
) / Science by SPA Fodor (1991) -
Pease, A.C. et al. Light-generated oligonucleotide arrays for rapid DNA sequence analysis. Proc. Natl. Acad. Sci. USA 91, 5022–5026 (1994).
(
10.1073/pnas.91.11.5022
) / Proc. Natl. Acad. Sci. USA by AC Pease (1994) -
Cronin, M.T. et al. Cystic fibrosis mutation detection by hybridization to light-generated DNA probe arrays. Hum. Mut. 7, 244–255 (1996).
(
10.1002/(SICI)1098-1004(1996)7:3<244::AID-HUMU9>3.0.CO;2-A
) / Hum. Mut. by MT Cronin (1996) - Lipshutz, R.J. et al. Using oligonucleotide arrays to probe genetic diversity. BioTechniques 19, 442–447 (1995). / BioTechniques by RJ Lipshutz (1995)
-
Kozal, M.J. et al. Extensive polymorphisms observed in HIV-1 clade B protease gene using high density oligonucleotide arrays. Nature Med. 2, 753–759 (1996).
(
10.1038/nm0796-753
) / Nature Med. by MJ Kozal (1996) -
Yershov, G. et al. DNA analysis and diagnostics on oligonucleotide microchips. Proc. Natl. Acad. Sci. USA 93, 491–4918 (1996).
(
10.1073/pnas.93.10.4913
) / Proc. Natl. Acad. Sci. USA by G Yershov (1996) -
Chee, M.S. et al. Accessing genetic information with high-density DNA arrays. Science 274, 610–614 (1996).
(
10.1126/science.274.5287.610
) / Science by MS Chee (1996) - Houldsworth, J. & Chaganti, R.S. Comparative genomic hybridization: an overview. Am. J. Pathol. 145, 1253–1260 (1994). / Am. J. Pathol. by J Houldsworth (1994)
-
Durocher, F. et al. Comparison of BRCA1 polymorphisms, rare sequence variants and/or missense mutations in unaffected and breast/ovarian cancer populations. Hum. Mol. Genet. 5, 835–842 (1996).
(
10.1093/hmg/5.6.835
) / Hum. Mol. Genet. by F Durocher (1996) -
Chapman, M.S. & Verma, I.M. Transcriptional activation by BRCA1 . Nature 382, 678–679 (1996).
(
10.1038/382678a0
) / Nature by MS Chapman (1996)
Dates
Type | When |
---|---|
Created | 21 years ago (Aug. 18, 2004, 4:13 p.m.) |
Deposited | 2 years, 3 months ago (May 18, 2023, 6:03 p.m.) |
Indexed | 2 months, 2 weeks ago (June 10, 2025, 3:04 p.m.) |
Issued | 28 years, 8 months ago (Dec. 1, 1996) |
Published | 28 years, 8 months ago (Dec. 1, 1996) |
Published Print | 28 years, 8 months ago (Dec. 1, 1996) |
@article{Hacia_1996, title={Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two–colour fluorescence analysis}, volume={14}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/ng1296-441}, DOI={10.1038/ng1296-441}, number={4}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Hacia, Joseph G. and Brody, Lawrence C. and Chee, Mark S. and Fodor, Stephen P.A. and Collins, Francis S.}, year={1996}, month=dec, pages={441–447} }