-
1
-
-
0031612929
-
Recommendations for a nomenclature system for human gene mutations
-
Antonarakis SE. 1998. Recommendations for a nomenclature system for human gene mutations. Nomenclature Working Group. Hum Mutat 11:1-3.
-
(1998)
Nomenclature Working Group. Hum Mutat
, vol.11
, pp. 1-3
-
-
Antonarakis, S.E.1
-
2
-
-
0028148889
-
Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer
-
Castilla LH, Couch FJ, Erdos MR, Hoskins KF, Calzone K, Garber JE, Boyd J, Lubin MB, Deshano ML, Brody LC, Collins FS, Weber BL. 1994. Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer. Nat Genet 8:387-391.
-
(1994)
Nat Genet
, vol.8
, pp. 387-391
-
-
Castilla, L.H.1
Couch, F.J.2
Erdos, M.R.3
Hoskins, K.F.4
Calzone, K.5
Garber, J.E.6
Boyd, J.7
Lubin, M.B.8
Deshano, M.L.9
Brody, L.C.10
Collins, F.S.11
Weber, B.L.12
-
3
-
-
0026092912
-
Genetic analysis of breast cancer in the cancer and steroid hormone study
-
Claus EB, Risch N, Thompson WD. 1991. Genetic analysis of breast cancer in the cancer and steroid hormone study. Am J Hum Genet 48:232-242.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 232-242
-
-
Claus, E.B.1
Risch, N.2
Thompson, W.D.3
-
5
-
-
0028999258
-
Ha-ras rare alleles in breast cancer susceptibility
-
Conway K, Edmiston S, Fried DB, Hulka BS, Garrett PA, Liu ET. 1995. Ha-ras rare alleles in breast cancer susceptibility. Breast Cancer Res Treat 35:97-104.
-
(1995)
Breast Cancer Res Treat
, vol.35
, pp. 97-104
-
-
Conway, K.1
Edmiston, S.2
Fried, D.B.3
Hulka, B.S.4
Garrett, P.A.5
Liu, E.T.6
-
6
-
-
0029980129
-
Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene
-
Couch FJ, Weber BL. 1996. Mutations and polymorphisms in the familial early-onset breast cancer (BRCA1) gene. Breast Cancer Information Core. Hum Mutat 8:8-18.
-
(1996)
Breast Cancer Information Core. Hum Mutat
, vol.8
, pp. 8-18
-
-
Couch, F.J.1
Weber, B.L.2
-
7
-
-
0031883606
-
Genetics of Cowden syndrome: Through the looking glass of oncology
-
Eng C. 1998. Genetics of Cowden syndrome: through the looking glass of oncology. Int J Oncol 12:701-710.
-
(1998)
Int J Oncol
, vol.12
, pp. 701-710
-
-
Eng, C.1
-
8
-
-
0028034348
-
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
-
Friedman LS, Ostermeyer EA, Szabo CI, Dowd P, Lynch ED, Rowell SE, King MC. 1994. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat Genet 8:399-404.
-
(1994)
Nat Genet
, vol.8
, pp. 399-404
-
-
Friedman, L.S.1
Ostermeyer, E.A.2
Szabo, C.I.3
Dowd, P.4
Lynch, E.D.5
Rowell, S.E.6
King, M.C.7
-
9
-
-
17944388284
-
Breast cancer information on the web
-
Friend S, Borresen AL, Brody L, Casey G, Devilee P, Gayther S, Goldgar D, Murphy P, Weber BL, Wiseman R. 1995. Breast cancer information on the web [letter]. Nat Genet 11:238-239.
-
(1995)
Nat Genet
, vol.11
, pp. 238-239
-
-
Friend, S.1
Borresen, A.L.2
Brody, L.3
Casey, G.4
Devilee, P.5
Gayther, S.6
Goldgar, D.7
Murphy, P.8
Weber, B.L.9
Wiseman, R.10
-
10
-
-
0025613812
-
Linkage of early-onset familial breast cancer to chromosome 17q21
-
Hall JM, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, King MC. 1990. Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250:1684-1689.
-
(1990)
Science
, vol.250
, pp. 1684-1689
-
-
Hall, J.M.1
Lee, M.K.2
Newman, B.3
Morrow, J.E.4
Anderson, L.A.5
Huey, B.6
King, M.C.7
-
11
-
-
0033987778
-
The human gene mutation data-base: A biomedical information and research resource
-
Krawczak M, Ball EV, Fenton I, Stenson PD, Abeysinghe S, Thomas N, Cooper DN. 2000. The human gene mutation data-base: a biomedical information and research resource. Hum Mutat 15:45-51.
-
(2000)
Hum Mutat
, vol.15
, pp. 45-51
-
-
Krawczak, M.1
Ball, E.V.2
Fenton, I.3
Stenson, P.D.4
Abeysinghe, S.5
Thomas, N.6
Cooper, D.N.7
-
12
-
-
0033021504
-
Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene
-
Meyn MS. 1999. Ataxia-telangiectasia, cancer and the pathobiology of the ATM gene. Clin Genet 55:289-304.
-
(1999)
Clin Genet
, vol.55
, pp. 289-304
-
-
Meyn, M.S.1
-
13
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian K, Liu Q, Cochran C, Bennett LM, Ding W, Bell R, Rosenthal J, Hussey C, Tran T, McClure M, Frye C, Hattier T, Phelps R, Haugen-Strano A, Katcher H, Yakumo K, Gholami Z, Shaffer D, Stone S, Bayer S, Wray C, Bogden R, Dayananth P, Ward J, Tonin P, Narod S, Bristow PK, Norris FH, Helvering L, Morrison P, Rosteck P, Lai M, Barrett JC, Lewis C, Neuhausen S, Cannon-Albright L, Goldgar D, Wiseman R, Kamb A, Skolnick MH. 1994. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266:66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, K.6
Liu, Q.7
Cochran, C.8
Bennett, L.M.9
Ding, W.10
Bell, R.11
Rosenthal, J.12
Hussey, C.13
Tran, T.14
McClure, M.15
Frye, C.16
Hattier, T.17
Phelps, R.18
Haugen-Strano, A.19
Katcher, H.20
Yakumo, K.21
Gholami, Z.22
Shaffer, D.23
Stone, S.24
Bayer, S.25
Wray, C.26
Bogden, R.27
Dayananth, P.28
Ward, J.29
Tonin, P.30
Narod, S.31
Bristow, P.K.32
Norris, F.H.33
Helvering, L.34
Morrison, P.35
Rosteck, P.36
Lai, M.37
Barrett, J.C.38
Lewis, C.39
Neuhausen, S.40
Cannon-Albright, L.41
Goldgar, D.42
Wiseman, R.43
Kamb, A.44
Skolnick, M.H.45
more..
-
14
-
-
0033566173
-
Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families
-
Montagna M, Santacatterina M, Torri A, Menin C, Zullato D, Chieco-Bianchi L, D'Andrea E. 1999. Identification of a 3 kb Alu-mediated BRCA1 gene rearrangement in two breast/ovarian cancer families. Oncogene 18:4160-4165.
-
(1999)
Oncogene
, vol.18
, pp. 4160-4165
-
-
Montagna, M.1
Santacatterina, M.2
Torri, A.3
Menin, C.4
Zullato, D.5
Chieco-Bianchi, L.6
D'Andrea, E.7
-
15
-
-
0030138354
-
Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer
-
Neuhausen S, Gilewski T, Norton L, Tran T, McGuire P, Swensen J, Hampel H, Borgen P, Brown K, Skolnick M, Shattuck-Eidens D, Jhanwar S, Goldgar D, Offit K. 1996a. Recurrent BRCA2 6174delT mutations in Ashkenazi Jewish women affected by breast cancer. Nat Genet 13:126-128.
-
(1996)
Nat Genet
, vol.13
, pp. 126-128
-
-
Neuhausen, S.1
Gilewski, T.2
Norton, L.3
Tran, T.4
McGuire, P.5
Swensen, J.6
Hampel, H.7
Borgen, P.8
Brown, K.9
Skolnick, M.10
Shattuck-Eidens, D.11
Jhanwar, S.12
Goldgar, D.13
Offit, K.14
-
16
-
-
19144362921
-
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: Results of an international study
-
Neuhausen SL, Mazoyer S, Friedman L, Stratton M, Offit K, Caligo A, Tomlinson G, Cannon-Albright L, Bishop T, Kelsell D, Solomon E, Weber B, Couch F, Struewing J, Tonin P, Durocher F, Narod S, Skolnick MH, Lenoir G, Serova O, Ponder B, Stoppa-Lyonnet D, Easton D, King MC, Goldgar DE. 1996b. Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study. Am J Hum Genet 58:271-280.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 271-280
-
-
Neuhausen, S.L.1
Mazoyer, S.2
Friedman, L.3
Stratton, M.4
Offit, K.5
Caligo, A.6
Tomlinson, G.7
Cannon-Albright, L.8
Bishop, T.9
Kelsell, D.10
Solomon, E.11
Weber, B.12
Couch, F.13
Struewing, J.14
Tonin, P.15
Durocher, F.16
Narod, S.17
Skolnick, M.H.18
Lenoir, G.19
Serova, O.20
Ponder, B.21
Stoppa-Lyonnet, D.22
Easton, D.23
King, M.C.24
Goldgar, D.E.25
more..
-
17
-
-
17344372404
-
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: Results of an international study
-
Neuhausen SL, Godwin AK, Gershoni-Baruch R, Schubert E, Garber J, Stoppa-Lyonnet D, Olah E, Csokay B, Serova O, Lalloo F, Osorio A, Stratton M, Offit K, Boyd J, Caligo MA, Scott RJ, Schofield A, Teugels E, Schwab M, Cannon-Albright L, Bishop T, Easton D, Benitez J, King MC, Ponder BAJ, Weber B, Devilee P, Borg A, Narod S, Goldgar D. 1998. Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study. Am J Hum Genet 62:1381-1388.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1381-1388
-
-
Neuhausen, S.L.1
Godwin, A.K.2
Gershoni-Baruch, R.3
Schubert, E.4
Garber, J.5
Stoppa-Lyonnet, D.6
Olah, E.7
Csokay, B.8
Serova, O.9
Lalloo, F.10
Osorio, A.11
Stratton, M.12
Offit, K.13
Boyd, J.14
Caligo, M.A.15
Scott, R.J.16
Schofield, A.17
Teugels, E.18
Schwab, M.19
Cannon-Albright, L.20
Bishop, T.21
Easton, D.22
Benitez, J.23
King, M.C.24
Ponder, B.A.J.25
Weber, B.26
Devilee, P.27
Borg, A.28
Narod, S.29
Goldgar, D.30
more..
-
18
-
-
2742525287
-
Inheritance of human breast cancer: Evidence for autosomal dominant transmission in high-risk families
-
Newman B, Austin MA, Lee M, King MC. 1988. Inheritance of human breast cancer: evidence for autosomal dominant transmission in high-risk families. Proc Natl Acad Sci USA 85:3044-3048.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 3044-3048
-
-
Newman, B.1
Austin, M.A.2
Lee, M.3
King, M.C.4
-
19
-
-
0032054311
-
A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ ovarian cancer family
-
Nordling M, Karlsson P, Wahlstrom J, Engwall Y, Wallgren A, Martinsson T. 1998. A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ ovarian cancer family. Cancer Res 58:1372-1375.
-
(1998)
Cancer Res
, vol.58
, pp. 1372-1375
-
-
Nordling, M.1
Karlsson, P.2
Wahlstrom, J.3
Engwall, Y.4
Wallgren, A.5
Martinsson, T.6
-
20
-
-
16044366988
-
The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%
-
Oddoux C, Struewing JP, Clayton CM, Neuhausen S, Brody LC, Kaback M, Haas B, Norton L, Borgen P, Jhanwar S, Goldgar D, Ostrer H, Offit K. 1996. The carrier frequency of the BRCA2 6174delT mutation among Ashkenazi Jewish individuals is approximately 1%. Nat Genet 14:188-190.
-
(1996)
Nat Genet
, vol.14
, pp. 188-190
-
-
Oddoux, C.1
Struewing, J.P.2
Clayton, C.M.3
Neuhausen, S.4
Brody, L.C.5
Kaback, M.6
Haas, B.7
Norton, L.8
Borgen, P.9
Jhanwar, S.10
Goldgar, D.11
Ostrer, H.12
Offit, K.13
-
21
-
-
0033559933
-
Estimates of the worldwide incidence of 25 major cancers in 1990
-
Parkin DM, Pisani P, Ferlay J. 1999. Estimates of the worldwide incidence of 25 major cancers in 1990. Int J Cancer 80:827-841.
-
(1999)
Int J Cancer
, vol.80
, pp. 827-841
-
-
Parkin, D.M.1
Pisani, P.2
Ferlay, J.3
-
22
-
-
16944363592
-
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients
-
Petrij-Bosch A, Peelen T, van Vliet M, van Eijk R, Olmer R, Drusedau M, Hogervorst FB, Hageman S, Arts PJ, Ligtenberg MJ, Meijers-Heijboer H, Klijn JG, Vasen HF, Cornelisse CJ, van't Veer LJ, Bakker E, van Ommen GJ, Devilee P. 1997. BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nat Genet 17:341-345.
-
(1997)
Nat Genet
, vol.17
, pp. 341-345
-
-
Petrij-Bosch, A.1
Peelen, T.2
Van Vliet, M.3
Van Eijk, R.4
Olmer, R.5
Drusedau, M.6
Hogervorst, F.B.7
Hageman, S.8
Arts, P.J.9
Ligtenberg, M.J.10
Meijers-Heijboer, H.11
Klijn, J.G.12
Vasen, H.F.13
Cornelisse, C.J.14
Van't Veer, L.J.15
Bakker, E.16
Van Ommen, G.J.17
Devilee, P.18
-
23
-
-
0030137718
-
Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families
-
Phelan CM, Lancaster JM, Tonin P, Gumbs C, Cochran C, Carter R, Ghadirian P, Perret C, Moslehi R, Dion F, Faucher MC, Dole K, Karimi S, Foulkes W, Lounis H, Warner E, GOSS P, Anderson D, Larsson C, Narod SA, Futreal PA. 1996. Mutation analysis of the BRCA2 gene in 49 site-specific breast cancer families. Nat Genet 13:120-122.
-
(1996)
Nat Genet
, vol.13
, pp. 120-122
-
-
Phelan, C.M.1
Lancaster, J.M.2
Tonin, P.3
Gumbs, C.4
Cochran, C.5
Carter, R.6
Ghadirian, P.7
Perret, C.8
Moslehi, R.9
Dion, F.10
Faucher, M.C.11
Dole, K.12
Karimi, S.13
Foulkes, W.14
Lounis, H.15
Warner, E.16
Goss, P.17
Anderson, D.18
Larsson, C.19
Narod, S.A.20
Futreal, P.A.21
more..
-
24
-
-
0032768930
-
The role of the p53 tumour suppressor gene in human breast cancer
-
Phillips HA. 1999. The role of the p53 tumour suppressor gene in human breast cancer. Clin Oncol 11:148-155.
-
(1999)
Clin Oncol
, vol.11
, pp. 148-155
-
-
Phillips, H.A.1
-
25
-
-
0031035045
-
A 1-kb alu-mediated germ-line deletion removing BRCA1 exon 17
-
Puget N, Torchard D, Serova-Sinilnikova OM, Lynch HT, Feunteun J, Lenoir GM, Mazoyer S. 1997. A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17. Cancer Res 57:828-831.
-
(1997)
Cancer Res
, vol.57
, pp. 828-831
-
-
Puget, N.1
Torchard, D.2
Serova-Sinilnikova, O.M.3
Lynch, H.T.4
Feunteun, J.5
Lenoir, G.M.6
Mazoyer, S.7
-
26
-
-
0033556051
-
Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions
-
Puget N, Stoppa-Lyonnet D, Sinilnikova OM, Pages S, Lynch HT, Lenoir GM, Mazoyer S. 1999. Screening for germ-line rearrangements and regulatory mutations in BRCA1 led to the identification of four new deletions. Cancer Res 59:455-461.
-
(1999)
Cancer Res
, vol.59
, pp. 455-461
-
-
Puget, N.1
Stoppa-Lyonnet, D.2
Sinilnikova, O.M.3
Pages, S.4
Lynch, H.T.5
Lenoir, G.M.6
Mazoyer, S.7
-
27
-
-
0029794992
-
Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2
-
Roa BB, Boyd AA, Volcik K, Richards CS. 1996. Ashkenazi Jewish population frequencies for common mutations in BRCA1 and BRCA2. Nat Genet 14:185-187.
-
(1996)
Nat Genet
, vol.14
, pp. 185-187
-
-
Roa, B.B.1
Boyd, A.A.2
Volcik, K.3
Richards, C.S.4
-
28
-
-
0028834145
-
A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening
-
Shattuck-Eidens D, McClure M, Simard J, Labrie F, Narod S, Couch F, Hoskins K, Weber B, Castilla L, Erdos M, Brody L, Friedman L, Ostermeyer E, Szabo C, King M-K, Jhanwar S, Offit K, Norton L, Gilewski T, Lubin M, Osborne M, Black D, Boyd M, Steel M, Ingles S, Haile R, Lindblom A, Olsson H, Borg A, Bishop DT, Solomon E, Radice P, Spatti G, Gayther S, Ponder B, Warren W, Stratton M, Liu Q, Fujimura F, Lewis C, Skolnick MH, Goldgar DE. 1995. A collaborative survey of 80 mutations in the BRCA1 breast and ovarian cancer susceptibility gene. Implications for presymptomatic testing and screening. JAMA 273:535-541.
-
(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
Hoskins, K.7
Weber, B.8
Castilla, L.9
Erdos, M.10
Brody, L.11
Friedman, L.12
Ostermeyer, E.13
Szabo, C.14
King, M.-K.15
Jhanwar, S.16
Offit, K.17
Norton, L.18
Gilewski, T.19
Lubin, M.20
Osborne, M.21
Black, D.22
Boyd, M.23
Steel, M.24
Ingles, S.25
Haile, R.26
Lindblom, A.27
Olsson, H.28
Borg, A.29
Bishop, D.T.30
Solomon, E.31
Radice, P.32
Spatti, G.33
Gayther, S.34
Ponder, B.35
Warren, W.36
Stratton, M.37
Liu, Q.38
Fujimura, F.39
Lewis, C.40
Skolnick, M.H.41
Goldgar, D.E.42
more..
-
29
-
-
0027939506
-
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families
-
Simard J, Tonin P, Durocher F, Morgan K, Rommens J, Gingras S, Samson C, Leblanc JF, Belanger C, Dion F, et al. 1994. Common origins of BRCA1 mutations in Canadian breast and ovarian cancer families. Nat Genet 8:392-398.
-
(1994)
Nat Genet
, vol.8
, pp. 392-398
-
-
Simard, J.1
Tonin, P.2
Durocher, F.3
Morgan, K.4
Rommens, J.5
Gingras, S.6
Samson, C.7
Leblanc, J.F.8
Belanger, C.9
Dion, F.10
-
30
-
-
0029804093
-
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1
-
Smith TM, Lee MK, Szabo CI, Jerome N, McEuen M, Taylor M, Hood L, King MC. 1996. Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1. Genome Res 6:1029-1049.
-
(1996)
Genome Res
, vol.6
, pp. 1029-1049
-
-
Smith, T.M.1
Lee, M.K.2
Szabo, C.I.3
Jerome, N.4
McEuen, M.5
Taylor, M.6
Hood, L.7
King, M.C.8
-
32
-
-
0029083814
-
The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals
-
Struewing JP, Abeliovich D, Peretz T, Avishai N, Kaback MM, Collins FS, Brody LC. 1995. The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals. Nat Genet 11:198-200.
-
(1995)
Nat Genet
, vol.11
, pp. 198-200
-
-
Struewing, J.P.1
Abeliovich, D.2
Peretz, T.3
Avishai, N.4
Kaback, M.M.5
Collins, F.S.6
Brody, L.C.7
-
33
-
-
0030869406
-
Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family
-
Swensen J, Hoffman M, Skolnick MH, Neuhausen SL. 1997. Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family. Hum Mol Genet 6:1513-1517.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1513-1517
-
-
Swensen, J.1
Hoffman, M.2
Skolnick, M.H.3
Neuhausen, S.L.4
-
34
-
-
0030902227
-
Population genetics of BRCA1 and BRCa2
-
Szabo CI, King MC. 1997. Population genetics of BRCA1 and BRCA2. Am J Hum Genet 60:1013-1020.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1013-1020
-
-
Szabo, C.I.1
King, M.C.2
-
35
-
-
13344269668
-
The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds
-
Tavtigian SV, Simard J, Rommens J, Couch F, Shattuck-Eidens D, Neuhausen S, Merajver S, Thorlacius S, Offit K, Stoppa-Lyonnet D, Belanger C, Bell R, Berry S, Bogden R, Chen Q, Davis T, Dumont M, Frye C, Hattier T, Jammulapati S, Janecki T, Jiang P, Kehrer R, Leblanc JF, Mitchell JT, McArthur-Morrison J, Nguyen K, Peng Y, Samson C, Schroeder M, Snyder SC, Steele L, Stringfellow M, Stroup C, Swedlund B, Swensen J, Teng D, Thomas A, Tran T, Tranchant M, Weaver-Feldhaus J, Wong AKC, Shizuya H, Eyfjord JE, Cannon-Albright L, Labrie F, Skolnick MH, Weber B, Kamb A, Goldgar DE. 1996. The complete BRCA2 gene and mutations in chromosome 13q-linked kindreds. Nat Genet 12:333-337.
-
(1996)
Nat Genet
, vol.12
, pp. 333-337
-
-
Tavtigian, S.V.1
Simard, J.2
Rommens, J.3
Couch, F.4
Shattuck-Eidens, D.5
Neuhausen, S.6
Merajver, S.7
Thorlacius, S.8
Offit, K.9
Stoppa-Lyonnet, D.10
Belanger, C.11
Bell, R.12
Berry, S.13
Bogden, R.14
Chen, Q.15
Davis, T.16
Dumont, M.17
Frye, C.18
Hattier, T.19
Jammulapati, S.20
Janecki, T.21
Jiang, P.22
Kehrer, R.23
Leblanc, J.F.24
Mitchell, J.T.25
McArthur-Morrison, J.26
Nguyen, K.27
Peng, Y.28
Samson, C.29
Schroeder, M.30
Snyder, S.C.31
Steele, L.32
Stringfellow, M.33
Stroup, C.34
Swedlund, B.35
Swensen, J.36
Teng, D.37
Thomas, A.38
Tran, T.39
Tranchant, M.40
Weaver-Feldhaus, J.41
Wong, A.K.C.42
Shizuya, H.43
Eyfjord, J.E.44
Cannon-Albright, L.45
Labrie, F.46
Skolnick, M.H.47
Weber, B.48
Kamb, A.49
Goldgar, D.E.50
more..
-
36
-
-
0030140026
-
A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes
-
Thorlacius S, Olafsdottir G, Tryggvadottir L, Neuhausen S, Jonasson JG, Tavtigian SV, Tulinius H, Ogmundsdottir HM, Eyfjord JE. 1996b. A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Nat Genet 13:117-119.
-
(1996)
Nat Genet
, vol.13
, pp. 117-119
-
-
Thorlacius, S.1
Olafsdottir, G.2
Tryggvadottir, L.3
Neuhausen, S.4
Jonasson, J.G.5
Tavtigian, S.V.6
Tulinius, H.7
Ogmundsdottir, H.M.8
Eyfjord, J.E.9
-
37
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, Fields P, Marshall G, Narod S, Lenoir GM, Lynch H, Feunteun J, Devilee P, Cornelisse CJ, Menko FH, Daly PA, Ormiston W, McManus R, Pye C, Lewis CM, Cannon-Albright LA, Peto J, Ponder BAJ, Skolnick MH, Easton DF, Goldgar DE, Stratton MR. 1994. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 265:2088-2090.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Ormiston, W.21
McManus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
38
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J, Swift S, Seal S, Mangion J, Collins N, Gregory S, Gumbs C, Micklem G. 1995. Identification of the breast cancer susceptibility gene BRCA2. Nature 378:789-792.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
Swift, S.4
Seal, S.5
Mangion, J.6
Collins, N.7
Gregory, S.8
Gumbs, C.9
Micklem, G.10
|