-
1
-
-
17344365851
-
Genetic heterogeneity and penetrance analysis of the BRCAI and BKCA2 genes in breast cancer families
-
Ford, D., Easton, D. F., Stratton, M., Narod, S . Goldgar, D., Devilee, P., Bishop, D. T., Weber, B., Lenoir, G., Chang-Claude, J., Sobol, H., Teare, M. D., Struewing, J., Arason, A., Scherneck, S., Peto, J., Rebbeck, T. R., Tonin, P., Neuhausen, S., Barkardottir, R., Eyfjord, J., Lynch, H., Ponder, B. A., Gayther, S. A., Birch, J. M., Lindblom, A., Stoppa-Lyonnet, D., Bignon, Y., Borg, A., Hamann, U., Haites, N., Scott, R. J. Maugard, C. M., Vasen, H., Seitz, S., Cannon-Albright, L. A., Schofield, A., Zelada-Hedman, M., and the Breast Cancer Linkage Consortium. Genetic heterogeneity and penetrance analysis of the BRCAI and BKCA2 genes in breast cancer families. Am. J. Hum. Genet., 62: 676-689, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 676-689
-
-
Ford, D.1
Easton, D.F.2
Stratton, M.3
Narod, S.4
Goldgar, D.5
Devilee, P.6
Bishop, D.T.7
Weber, B.8
Lenoir, G.9
Chang-Claude, J.10
Sobol, H.11
Teare, M.D.12
Struewing, J.13
Arason, A.14
Scherneck, S.15
Peto, J.16
Rebbeck, T.R.17
Tonin, P.18
Neuhausen, S.19
Barkardottir, R.20
Eyfjord, J.21
Lynch, H.22
Ponder, B.A.23
Gayther, S.A.24
Birch, J.M.25
Lindblom, A.26
Stoppa-Lyonnet, D.27
Bignon, Y.28
Borg, A.29
Hamann, U.30
Haites, N.31
Scott, R.J.32
Maugard, C.M.33
Vasen, H.34
Seitz, S.35
Cannon-Albright, L.A.36
Schofield, A.37
Zelada-Hedman, M.38
more..
-
2
-
-
0031035045
-
1-kb Alu-mediated germ-line deletion removing BKCA1 exon 17
-
Puget, N., Torchard, D., Serova-Sinilnikova, O. M., Lynch, H. T., Feunteun, J., Lenoir, G. M., and Mazoyer, S. A 1-kb Alu-mediated germ-line deletion removing BKCA1 exon 17. Cancer Res., 57: 828-831, 1997.
-
(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.A.7
-
3
-
-
0030869406
-
Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family
-
Swensen, J., Hoffman, M., Skolnick, M. H., and Neuhausen, S. L. Identification of a 14 kb deletion involving the promoter region of BRCA1 in a breast cancer family. Hum. Mol. Genet., 6: 1513-1517, 1997.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1513-1517
-
-
Swensen, J.1
Hoffman, M.2
Skolnick, M.H.3
Neuhausen, S.L.4
-
4
-
-
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, F. B., Hageman, S., Arts, P. J., Ligtenberg, M. J., Meijers-Heijboer, H., Klijn, J. G., Vasen, H. F., Cornelisse, C. J., van't Veer, L. J., Balder, E., van Ommen, G. J., and Devilee. P. BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients. Nat. Genet., 17: 341-345, 1997.
-
(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
Balder, E.16
Van Ommen, G.J.17
Devilee, P.18
-
5
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Washington DC
-
Miki, Y., Swensen, J., Shattuck-Eidens, D., Futreal, P. A., Harshman, K., Tavtigian, S., Liu, Q., Cochran, C., Bennett, L. M., 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., Dayanamh, P., Ward, J., Tonin, P., Narod, S., Bristow, P. K., Norris, F. H., Helvering, L., Morrison, P., Rosteck, P., Lai, M., Barrett, J. C., Lewis, C., Neuhausen, S., Cannon-Albright, L., Goldgar, D., Wiseman, R., Kamb, A., and Skolnick, M. H. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science (Washington DC), 266: 66-71, 1994.
-
(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, S.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
Dayanamh, 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..
-
6
-
-
0028844202
-
Germline mutations of the BRCA1 gene in breast/ovarian cancer families: Evidence for a genotype/phenotype correlation
-
Gayther, S. A., Warren, W., Mazoyer, S., Russell, P. A., Harrington, P. A., Chiano, M., Seal, S., Hamoudi, R., van Rensburg, E. J., Dunning, A. M., Love, R., Evans, G., Easton, D., Clayton, D., Stralton, M. R., and Ponder, B. A. J. Germline mutations of the BRCA1 gene in breast/ovarian cancer families: evidence for a genotype/phenotype correlation. Nat. Genet., 11:428-433, 1995.
-
(1995)
Nat. Genet.
, vol.11
, pp. 428-433
-
-
Gayther, S.A.1
Warren, W.2
Mazoyer, S.3
Russell, P.A.4
Harrington, P.A.5
Chiano, M.6
Seal, S.7
Hamoudi, R.8
Van Rensburg, E.J.9
Dunning, A.M.10
Love, R.11
Evans, G.12
Easton, D.13
Clayton, D.14
Stralton, M.R.15
Ponder, B.A.J.16
-
7
-
-
0031033343
-
Mutations and alternative splicing of the BRCA1 gene in U.K. Breast/ovarian cancer families
-
Xu, C-F., Chambers, J. A., Nicolai, H., Brown, M. A., Hujeirat, Y., Mohammed, S., Hodgson, S., Kelsell, D. P., Spurr, N. K., Bishop, D. T., and Solomon, E. Mutations and alternative splicing of the BRCA1 gene in U.K. breast/ovarian cancer families. Genes Chromosomes Cancer. 18: 102-110, 1997.
-
(1997)
Genes Chromosomes Cancer.
, vol.18
, pp. 102-110
-
-
Xu, C.-F.1
Chambers, J.A.2
Nicolai, H.3
Brown, M.A.4
Hujeirat, Y.5
Mohammed, S.6
Hodgson, S.7
Kelsell, D.P.8
Spurr, N.K.9
Bishop, D.T.10
Solomon, E.11
-
8
-
-
0029655346
-
A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families
-
Serova, O., Montagna, M., Torchard, D., Narod, S. A., Tonin, P., Sylla, B., Lynch, H. T., Feunteun, J., and Lenoir, G. M. A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families. Am. J. Hum. Genet., 58: 42-51, 1996.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 42-51
-
-
Serova, O.1
Montagna, M.2
Torchard, D.3
Narod, S.A.4
Tonin, P.5
Sylla, B.6
Lynch, H.T.7
Feunteun, J.8
Lenoir, G.M.9
-
9
-
-
16944361810
-
Mutations in BRCA1 and BRCA2 in breast cancer families: Are there more genes?
-
Serova, O., Maroyer, S., Puget, N., Dubois, V., Tonin, P., Shugart, Y. Y., Goldgar, D. E., Narod, S. A., Lynch, H. T., and Lenoir, G. M. Mutations in BRCA1 and BRCA2 in breast cancer families: are there more genes? Am. J. Hum. Genet., 60: 486-495, 1997.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 486-495
-
-
Serova, O.1
Maroyer, S.2
Puget, N.3
Dubois, V.4
Tonin, P.5
Shugart, Y.Y.6
Goldgar, D.E.7
Narod, S.A.8
Lynch, H.T.9
Lenoir, G.M.10
-
10
-
-
16944364123
-
BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic
-
Stoppa-Lyonnet, D., Laurent-Puig, P., Essioux, L., Pages, S., Ithier, G., Ligot, L., Fourquet, A.. Salmon, R. J., Clough, K. B., Pouillart, P., the Institut Curie Breast Cancer Group. Bonaiti-Pellic, C., and Thomas, G. BRCA1 sequence variations in 160 individuals referred to a breast/ovarian family cancer clinic. Am. J. Hum. Genet., 60: 1021-1030, 1997.
-
(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
Fourquet, A.7
Salmon, R.J.8
Clough, K.B.9
Pouillart, P.10
Bonaiti-Pellic, C.11
Thomas, G.12
-
11
-
-
0029804093
-
Complete genomic sequence and analysis of 117 kb of human DNA containing the gene KRCA1
-
Smith, T. M., Lee, M. K., Szabo, C. I., Jerome, N., McEuen, M., Taylor, M., Hood, L., and King, M. C. Complete genomic sequence and analysis of 117 kb of human DNA containing the gene KRCA1. Genome Res., 6: 1029-1049, 1996.
-
(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
-
12
-
-
0004136246
-
-
Cold Spring Harbor, NY: Cold Spring Harbor Laboratory
-
Sambrook, J., Fritsch, E. F., and Maniatis, T. Molecular Cloning: A Laboratory Manual, Ed. 2. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual, Ed. 2
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
13
-
-
0028034348
-
Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families
-
Friedman, L. S., Ostermeyer, E. A., Szabo, C. I.. Dowd, P., Lynch, E. D., Rowell, S. E., and King, M-C. Confirmation of BRCA1 by analysis of germline mutations linked to breast and ovarian cancer in ten families. Nat. Genet., 8: 399-404, 1994.
-
(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
-
15
-
-
0027937794
-
A P1-based physical map of the region from D17s776 to D17s78 containing the breast cancer susceptibility gene BKCA1
-
Neuhausen, S. L., Swensen, J., Miki, Y., Liu, Q., Tavtigian, S., Shattuck-Eidens, D., Kamb, A., Hobbs, M. R., Gingrich, J., Shizuya, H., Kim, U-J., Cochran, C., Futreal, P. A., Wiseman, R. W., Lynch, H. T., Tonin, P., Narod, S., Cannon-Albright, L., Skolnick, M. H., and Goldgar, D. E. A P1-based physical map of the region from D17S776 to D17S78 containing the breast cancer susceptibility gene BKCA1. Hum. Mol. Genet., 3: 1919-1926, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1919-1926
-
-
Neuhausen, S.L.1
Swensen, J.2
Miki, Y.3
Liu, Q.4
Tavtigian, S.5
Shattuck-Eidens, D.6
Kamb, A.7
Hobbs, M.R.8
Gingrich, J.9
Shizuya, H.10
Kim, U.-J.11
Cochran, C.12
Futreal, P.A.13
Wiseman, R.W.14
Lynch, H.T.15
Tonin, P.16
Narod, S.17
Cannon-Albright, L.18
Skolnick, M.H.19
Goldgar, D.E.20
more..
-
16
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenhach, J., Gyapay, G., Dib, C., Vignal, A., Morissette, J., Millasseau, P., Vaysseix, G., and Lathrop, M. A second-generation linkage map of the human genome. Nature (Lond.), 359: 794-801, 1992.
-
(1992)
Nature (Lond.)
, vol.359
, pp. 794-801
-
-
Weissenhach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.V.6
Lathrop, M.7
-
17
-
-
0030761231
-
Complex regulation of the BRCA1 gene
-
Xu, C-F., Chambers, J. A., and Solomon, E. Complex regulation of the BRCA1 gene. J. Biol. Chem., 272: 20994-20997, 1997.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 20994-20997
-
-
Xu, C.-F.1
Chambers, J.A.2
And Solomon, E.3
-
18
-
-
0030799598
-
Isolation and characterisation of the NBK2 gene which lies head to head with the human BRCA1 gene
-
Xu, C-F., Brown, M. A., Nicolai, H., Chambers, J. A., Griffiths, B. L., and Solomon, E. Isolation and characterisation of the NBK2 gene which lies head to head with the human BRCA1 gene. Hum. Mol. Genet., 6: 1057-1062 1997.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1057-1062
-
-
Xu, C.-F.1
Brown, M.A.2
Nicolai, H.3
Chambers, J.A.4
Griffiths, B.L.5
Solomon, E.6
-
19
-
-
0028266931
-
MRNA translation: Influence of the 5′ and 3′ untranslated regions
-
Sonenberg, N. mRNA translation: influence of the 5′ and 3′ untranslated regions. Curr. Opin. Gen. Dev., 4: 310-315, 1994.
-
(1994)
Curr. Opin. Gen. Dev.
, vol.4
, pp. 310-315
-
-
Sonenberg, N.1
-
20
-
-
0025805209
-
Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma
-
Kloss, K., Währisch, P., Greger, V., Messmer, E., Fritze, H., Höpping, W., Passarge, E., and Horsthemke, B. Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastoma. Am. J. Med. Genet., 39: 196-200, 1991.
-
(1991)
Am. J. Med. Genet.
, vol.39
, pp. 196-200
-
-
Kloss, K.1
Währisch, P.2
Greger, V.3
Messmer, E.4
Fritze, H.5
Höpping, W.6
Passarge, E.7
Horsthemke, B.8
-
21
-
-
0028082464
-
Deletions spanning the neurofibromatosis 1 gene: Identification and phenotype of five patients
-
Kayes, L. M., Burke, W., Riccardi, V. M., Bennett, R., Ehrlich, P., Rubenstein, A., and Stephens, K. Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients. Am. J. Hum. Genet., 54: 424-436, 1994.
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 424-436
-
-
Kayes, L.M.1
Burke, W.2
Riccardi, V.M.3
Bennett, R.4
Ehrlich, P.5
Rubenstein, A.6
Stephens, K.7
-
22
-
-
0029964807
-
Characterization of a cytogenetic 17q11.2 deletion in an NK1 patient with a contiguous gene syndrome
-
Riva, P., Castorina, P., Manoukian, S., Dalpra, L., Doneda, L., Marini, G., den Dunnen, J., and Larizza, L. Characterization of a cytogenetic 17q11.2 deletion in an NK1 patient with a contiguous gene syndrome. Hum. Genet., 98: 646-650, 1996.
-
(1996)
Hum. Genet.
, vol.98
, pp. 646-650
-
-
Riva, P.1
Castorina, P.2
Manoukian, S.3
Dalpra, L.4
Doneda, L.5
Marini, G.6
Den Dunnen, J.7
Larizza, L.8
-
23
-
-
0028886723
-
Germline mutations in the von HippelLindau disease (VHL) gene in Japanese VHL
-
Clinical Research Group for VHL in Japan. Germline mutations in the von HippelLindau disease (VHL) gene in Japanese VHL. Hum. Mol. Genet., 4: 2233-2237, 1995.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2233-2237
-
-
-
24
-
-
0027933150
-
A physical map and candidate genes in the BRCA1 region on chromosome 17q12-21
-
Albertsen, H. M., Smith, S. A., Mazoyer, S., Fujimoto, E., Stevens, J. Williams, B., Rodriguez, P., Cropp, C. S., Slijepcevic, P., Carlson, M. Robertson, M., Bradley, P., Lawrence, E., Harrington, T., Mei Sheng, Z., Hoopes, R., Sternberg, N., Brothman, A., Callahan, R., Ponder, B. A. J., and White, R. A physical map and candidate genes in the BRCA1 region on chromosome 17q12-21. Nat. Genet., 7: 472-479, 1994.
-
(1994)
Nat. Genet.
, vol.7
, pp. 472-479
-
-
Albertsen, H.M.1
Smith, S.A.2
Mazoyer, S.3
Fujimoto, E.4
Stevens, J.5
Williams, B.6
Rodriguez, P.7
Cropp, C.S.8
Slijepcevic, P.9
Carlson, M.10
Robertson, M.11
Bradley, P.12
Lawrence, E.13
Harrington, T.14
Mei Sheng, Z.15
Hoopes, R.16
Sternberg, N.17
Brothman, A.18
Callahan, R.19
Ponder, B.A.J.20
White, R.21
more..
-
25
-
-
0029009410
-
Physical mapping, cloning, and identification of genes within a 500-kb region containing BRCA1
-
Brown, M. A., Jones, K. A., Nicolai, H., Bonjardim, M., Black, D., McFarlane, R., de Jong, P, Quirk, J. P., Lehrach, H., and Solomon, E. Physical mapping, cloning, and identification of genes within a 500-kb region containing BRCA1. Proc. Natl. Acad. Sci. USA, 92: 4362-4366, 1995.
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 4362-4366
-
-
Brown, M.A.1
Jones, K.A.2
Nicolai, H.3
Bonjardim, M.4
Black, D.5
McFarlane, R.6
De Jong, P.7
Quirk, J.P.8
Lehrach, H.9
Solomon, E.10
-
26
-
-
0028967353
-
One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi
-
Rüdiger, N. S., Gregersen, N., and Kiellend-Brandt, M. C. One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. Nucleic Acids Res., 23: 256-260, 1995.
-
(1995)
Nucleic Acids Res.
, vol.23
, pp. 256-260
-
-
Rüdiger, N.S.1
Gregersen, N.2
Kiellend-Brandt, M.C.3
-
27
-
-
0025174888
-
Clusters of intragenic Alu repeats predispose the human Cl inhibitor locus to deleterious rearrangements
-
Stoppa-Lyonnet, D., Carter, P. E., Meo, T., and Tosi, M. Clusters of intragenic Alu repeats predispose the human Cl inhibitor locus to deleterious rearrangements. Proc. Natl. Acad. Sci. USA, 87: 1551-1555, 1990.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 1551-1555
-
-
Stoppa-Lyonnet, D.1
Carter, P.E.2
Meo, T.3
Tosi, M.4
-
28
-
-
0025997032
-
Recombinational biases in the rearranged Cl-inhibitor genes of hereditary angioedema patients
-
Stoppa-Lyonnet, D., Duponchel, C., Meo, T., Laurent, J., Carter, P. E., Arala-Chaves, M., Cohen, J. H., Dewald, G., Goetz, J., Hauptmann, G., Lagrue, G., Lesavre, P., Lopez-Tracasa, M., Misiano, G., Moraine, C., Sobel, A., Späth, P. J., and Tosi, M. Recombinational biases in the rearranged Cl-inhibitor genes of hereditary angioedema patients. Am. J. Hum. Genet., 49: 1055-1062, 1991.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1055-1062
-
-
Stoppa-Lyonnet, D.1
Duponchel, C.2
Meo, T.3
Laurent, J.4
Carter, P.E.5
Arala-Chaves, M.6
Cohen, J.H.7
Dewald, G.8
Goetz, J.9
Hauptmann, G.10
Lagrue, G.11
Lesavre, P.12
Lopez-Tracasa, M.13
Misiano, G.14
Moraine, C.15
Sobel, A.16
Späth, P.J.17
Tosi, M.18
-
29
-
-
0031981818
-
A BRCA1 nonsense mutation causes exon skipping
-
Mazoyer, S., Puget, N., Perrin-Vidoz., L., Lynch, H. T., Serova-Sinilnikova, O. M., and Lenoir, G. M. A BRCA1 nonsense mutation causes exon skipping. Am. J. Hum. Genet., 62: 713-715, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 713-715
-
-
Mazoyer, S.1
Puget, N.2
Perrin-Vidoz, L.3
Lynch, H.T.4
Serova-Sinilnikova, O.M.5
Lenoir, G.M.6
-
30
-
-
0030852505
-
BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing
-
Shattuck-Eidens, D., Oliphant, A., McClure, M., McBride, C., Gupte, J., Rubano, T., Pruss, D., Tavtigian, S. V., Teng, D. H., Adey, N., Staebell, M., Gumpper, K., Lundstrom, R., Hulick, M., Kelly, M., Holmen, J., Lingenfelter, B., Manley, S., Fujimura, F., Luce, M., Ward, B., Cannon-Albright, L., Steele, L., Offit, K., Gilewski, T., Norton, L., Brown, K., Schulz, C., Hampel, H., Schluger, A., Giulotto, E., Zoli, W., Ravaioli, A., Nevanlinna, H., Pyrhonen, S., Rowley, P., Loader, S., Osborne, M. P.. Daly, M., Tepler, I., Weinstein, P. L., Scalia, J. L., Michaelson, R., Scott, R. J., Radice, P., Pierotti, M. A., Garber, J. E., Isaacs, C., Peshkin, B., Lippman, M. E., Dosik, M. H., Caligo, M. A., Greenstein, R. M., Pilarski, R., Weber, B. L., Burgemeister, R., Frank, T. S., Skolnick, M. H., and Thomas, A. BRCA1 sequence analysis in women at high risk for susceptibility mutations. Risk factor analysis and implications for genetic testing. J. Am. Med. Assoc., 278: 1242-1250, 1997.
-
(1997)
J. Am. Med. Assoc.
, vol.278
, pp. 1242-1250
-
-
Shattuck-Eidens, D.1
Oliphant, A.2
McClure, M.3
McBride, C.4
Gupte, J.5
Rubano, T.6
Pruss, D.7
Tavtigian, S.V.8
Teng, D.H.9
Adey, N.10
Staebell, M.11
Gumpper, K.12
Lundstrom, R.13
Hulick, M.14
Kelly, M.15
Holmen, J.16
Lingenfelter, B.17
Manley, S.18
Fujimura, F.19
Luce, M.20
Ward, B.21
Cannon-Albright, L.22
Steele, L.23
Offit, K.24
Gilewski, T.25
Norton, L.26
Brown, K.27
Schulz, C.28
Hampel, H.29
Schluger, A.30
Giulotto, E.31
Zoli, W.32
Ravaioli, A.33
Nevanlinna, H.34
Pyrhonen, S.35
Rowley, P.36
Loader, S.37
Osborne, M.P.38
Daly, M.39
Tepler, I.40
Weinstein, P.L.41
Scalia, J.L.42
Michaelson, R.43
Scott, R.J.44
Radice, P.45
Pierotti, M.A.46
Garber, J.E.47
Isaacs, C.48
Peshkin, B.49
Lippman, M.E.50
Dosik, M.H.51
Caligo, M.A.52
Greenstein, R.M.53
Pilarski, R.54
Weber, B.L.55
Burgemeister, R.56
Frank, T.S.57
Skolnick, M.H.58
Thomas, A.59
more..
|