-
1
-
-
0033011011
-
Update on the incidence and mortality from melanoma in the United States
-
Hall HI, Miller DR, Rogers JD, Bewerse B: Update on the incidence and mortality from melanoma in the United States. J Am Acad Dermatol 1999, 40(1):35-42.
-
(1999)
J. Am. Acad. Dermatol.
, vol.40
, Issue.1
, pp. 35-42
-
-
Hall, H.I.1
Miller, D.R.2
Rogers, J.D.3
Bewerse, B.4
-
2
-
-
0037724456
-
Cancer Facts and Figures 2002
-
American Cancer Society
-
American Cancer Society: Cancer Facts and Figures 2002. 2003 [http://www.cancer.org/downloads/STT/Cancer Facts&Figures2002TM.pdf].
-
(2003)
-
-
-
3
-
-
0141992252
-
The melanoma epidemic: Res ipsa loquitur
-
Beddingfield FC III: The melanoma epidemic: res ipsa loquitur. Oncologist 2003, 8(5):459-465.
-
(2003)
Oncologist
, vol.8
, Issue.5
, pp. 459-465
-
-
Beddingfield III, F.C.1
-
4
-
-
0028100903
-
Germline p16 mutations in familial melanoma
-
Hussussian CJ, Struewing JP, Goldstein AM, Higgins PA, Ally DS, Sheahan MD, Clark WH Jr, Tucker MA, Dracopoli NC: Germline p16 mutations in familial melanoma. Nat Genet 1994, 8(1):15-21.
-
(1994)
Nat. Genet.
, vol.8
, Issue.1
, pp. 15-21
-
-
Hussussian, C.J.1
Struewing, J.P.2
Goldstein, A.M.3
Higgins, P.A.4
Ally, D.S.5
Sheahan, M.D.6
Clark Jr., W.H.7
Tucker, M.A.8
Dracopoli, N.C.9
-
5
-
-
0028085975
-
Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus
-
Kamb A, Shattuck-Eidens D, Eeles R, Liu Q, Gruis NA, Ding W, Hussey C, Tran T, Miki Y, Weaver-Feldhaus J: Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus. Nat Genet 1994, 8(1):23-26.
-
(1994)
Nat. Genet.
, vol.8
, Issue.1
, pp. 23-26
-
-
Kamb, A.1
Shattuck-Eidens, D.2
Eeles, R.3
Liu, Q.4
Gruis, N.A.5
Ding, W.6
Hussey, C.7
Tran, T.8
Miki, Y.9
Weaver-Feldhaus, J.10
-
6
-
-
6844226190
-
Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France
-
The French Familial Melanoma Study Group
-
Soufir N, Avril MF, Chompret A, Demenais F, Bombled J, Spatz A, Stoppa-Lyonnet D, Benard J, Bressac-de Paillerets B: Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France. The French Familial Melanoma Study Group. Hum Mol Genet 1998, 7(2):209-216.
-
(1998)
Hum. Mol. Genet.
, vol.7
, Issue.2
, pp. 209-216
-
-
Soufir, N.1
Avril, M.F.2
Chompret, A.3
Demenais, F.4
Bombled, J.5
Spatz, A.6
Stoppa-Lyonnet, D.7
Benard, J.8
Bressac-de Paillerets, B.9
-
7
-
-
0038122762
-
Genetic Epidemiology of Melanoma
-
Bataille V: Genetic Epidemiology of Melanoma. Eur J Cancer 2003, 39(10):1341-1347.
-
(2003)
Eur. J. Cancer
, vol.39
, Issue.10
, pp. 1341-1347
-
-
Bataille, V.1
-
8
-
-
17544392528
-
Vitamin D receptor polymorphisms are associated with altered pro-gnosis in patients with malignant melanoma
-
Hutchinson PE, Osborne JE, Lear JT, Smith AG, Bowers PW, Morris PN, Jones PW, York C, Strange RC, Fryer AA: Vitamin D receptor polymorphisms are associated with altered pro-gnosis in patients with malignant melanoma. Clin Cancer Res 2000,6(2):498-504.
-
(2000)
Clin. Cancer Res.
, vol.6
, Issue.2
, pp. 498-504
-
-
Hutchinson, P.E.1
Osborne, J.E.2
Lear, J.T.3
Smith, A.G.4
Bowers, P.W.5
Morris, P.N.6
Jones, P.W.7
York, C.8
Strange, R.C.9
Fryer, A.A.10
-
9
-
-
7344236227
-
Susceptibility to melanoma: Influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene
-
Ichii-Jones F, Lear JT, Heagerty AH, Smith AG, Hutchinson PE, Osborne J, Bowers B, Jones PW, Davies E, Ollier WE, Thomson W, Yengi L, Bath J, Fryer AA, Strange RC: Susceptibility to melanoma: influence of skin type and polymorphism in the melanocyte stimulating hormone receptor gene. J Invest Dermatol 1998, 111(2):218-221.
-
(1998)
J. Invest. Dermatol.
, vol.111
, Issue.2
, pp. 218-221
-
-
Ichii-Jones, F.1
Lear, J.T.2
Heagerty, A.H.3
Smith, A.G.4
Hutchinson, P.E.5
Osborne, J.6
Bowers, B.7
Jones, P.W.8
Davies, E.9
Ollier, W.E.10
Thomson, W.11
Yengi, L.12
Bath, J.13
Fryer, A.A.14
Strange, R.C.15
-
10
-
-
0029839525
-
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma
-
Valverde P, Healy E, Sikkink S, Haldane F, Thody AJ, Carothers A, Jackson IJ, Rees JL: The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma. Hum Mol Genet 1996, 5(10):1663-1666.
-
(1996)
Hum. Mol. Genet.
, vol.5
, Issue.10
, pp. 1663-1666
-
-
Valverde, P.1
Healy, E.2
Sikkink, S.3
Haldane, F.4
Thody, A.J.5
Carothers, A.6
Jackson, I.J.7
Rees, J.L.8
-
11
-
-
0029156961
-
Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma
-
MMM group. Multi-disciplinary Malignant Melanoma Group
-
Lafuente A, Molina R, Palou J, Castel T, Moral A, Trias M: Phenotype of glutathione S-transferase Mu (GSTM1) and susceptibility to malignant melanoma. MMM group. Multi-disciplinary Malignant Melanoma Group. Br J Cancer 1995, 72(2):324-326.
-
(1995)
Br. J. Cancer
, vol.72
, Issue.2
, pp. 324-326
-
-
Lafuente, A.1
Molina, R.2
Palou, J.3
Castel, T.4
Moral, A.5
Trias, M.6
-
12
-
-
0032767989
-
Cytochrome P450 CYP2D6 genotypes: Association with hair colour, Breslow thickness and melanocyte stimulating hormone receptor alleles in patients with malignant melanoma
-
Strange RC, Ellison T, Ichii-Jones F, Bath J, Hoban P, Lear JT, Smith AG, Hutchinson PE, Osborne J, Bowers B, Jones PW, Fryer AA: Cytochrome P450 CYP2D6 genotypes: association with hair colour, Breslow thickness and melanocyte stimulating hormone receptor alleles in patients with malignant melanoma. Pharmacogenetics 1999, 9(3):269-276.
-
(1999)
Pharmacogenetics
, vol.9
, Issue.3
, pp. 269-276
-
-
Strange, R.C.1
Ellison, T.2
Ichii-Jones, F.3
Bath, J.4
Hoban, P.5
Lear, J.T.6
Smith, A.G.7
Hutchinson, P.E.8
Osborne, J.9
Bowers, B.10
Jones, P.W.11
Fryer, A.A.12
-
13
-
-
0037006414
-
Association between functional polymorphism in EGF gene and malignant melanoma
-
Shahbazi M, Pravica V, Nasreen N, Fakhoury H, Fryer AA, Strange RC, Hutchinson PE, Osborne JE, Lear JT, Smith AG, Hutchinson IV: Association between functional polymorphism in EGF gene and malignant melanoma. Lancet 2002, 359(9304):397-401.
-
(2002)
Lancet
, vol.359
, Issue.9304
, pp. 397-401
-
-
Shahbazi, M.1
Pravica, V.2
Nasreen, N.3
Fakhoury, H.4
Fryer, A.A.5
Strange, R.C.6
Hutchinson, P.E.7
Osborne, J.E.8
Lear, J.T.9
Smith, A.G.10
Hutchinson, I.V.11
-
14
-
-
0034486175
-
The genetics of cutaneous melanoma
-
Pollock PM, Trent JM: The genetics of cutaneous melanoma. Clin Lab Med 2000, 20(4):667-690.
-
(2000)
Clin. Lab. Med.
, vol.20
, Issue.4
, pp. 667-690
-
-
Pollock, P.M.1
Trent, J.M.2
-
15
-
-
0033518889
-
CDKN2A variants in a population-based sample of Queensland families with melanoma
-
Aitken J, Welch J, Duffy D, Milligan A, Green A, Martin N, Haywar N: CDKN2A variants in a population-based sample of Queensland families with melanoma. J Natl Cancer Inst 1999, 91(5):446-452.
-
(1999)
J. Natl. Cancer Inst.
, vol.91
, Issue.5
, pp. 446-452
-
-
Aitken, J.1
Welch, J.2
Duffy, D.3
Milligan, A.4
Green, A.5
Martin, N.6
Haywar, N.7
-
16
-
-
0033818195
-
Low prevalence of germline CDKN2A and CDK4 mutations in patients with early-onset melanoma
-
Tsao H, Zhang X, Kwitkiwski K, Finkelstein DM, Sober AJ, Haluska FG: Low prevalence of germline CDKN2A and CDK4 mutations in patients with early-onset melanoma. Arch Dermatol 2000, 136(9):1118-1122.
-
(2000)
Arch. Dermatol.
, vol.136
, Issue.9
, pp. 1118-1122
-
-
Tsao, H.1
Zhang, X.2
Kwitkiwski, K.3
Finkelstein, D.M.4
Sober, A.J.5
Haluska, F.G.6
-
17
-
-
0033039497
-
Prospects for whole-genome linkage disequilibrium mapping of common disease genes
-
Kruglyak L: Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nat Genet 1999, 22(2):139-144.
-
(1999)
Nat. Genet.
, vol.22
, Issue.2
, pp. 139-144
-
-
Kruglyak, L.1
-
18
-
-
0037168512
-
Association testing by DNA pooling: An effective initial screen
-
Bansal A, van den BD, Kammerer S, Honisch C, Adam G, Cantor CR, Kleyn P, Braun A: Association testing by DNA pooling: an effective initial screen. Proc Natl Acad Sci U S A 2002, 99(26):16871-16874.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, Issue.26
, pp. 16871-16874
-
-
Bansal, A.1
van den, B.D.2
Kammerer, S.3
Honisch, C.4
Adam, G.5
Cantor, C.R.6
Kleyn, P.7
Braun, A.8
-
19
-
-
0037168559
-
High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools
-
Mohlke KL, Erdos MR, Scott LJ, Fingerlin TE, Jackson AU, Silander K, Hollstein P, Boehnke M, Collins FS: High-throughput screening for evidence of association by using mass spectrometry genotyping on DNA pools. Proc Natl Acad Sci U S A 2002, 99(26):16928-16933.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, Issue.26
, pp. 16928-16933
-
-
Mohlke, K.L.1
Erdos, M.R.2
Scott, L.J.3
Fingerlin, T.E.4
Jackson, A.U.5
Silander, K.6
Hollstein, P.7
Boehnke, M.8
Collins, F.S.9
-
20
-
-
2942569420
-
Systematic Identification of Disease-Related Genes
-
Kammerer S, Langdown M, Roth R, Mah S, Hoyal C, Marnellos G, Reneland R, Nelson M, Braun A: Systematic Identification of Disease-Related Genes.2003 [http://www.sequenom.com/Assets/pdfs/posters].
-
(2003)
-
-
Kammerer, S.1
Langdown, M.2
Roth, R.3
Mah, S.4
Hoyal, C.5
Marnellos, G.6
Reneland, R.7
Nelson, M.8
Braun, A.9
-
21
-
-
0028107345
-
Signal transduction pathways involving the Raf proto-oncogene
-
Williams NG, Roberts TM: Signal transduction pathways involving the Raf proto-oncogene. Cancer Metastasis Rev 1994, 13(1):105-116.
-
(1994)
Cancer Metastasis Rev.
, vol.13
, Issue.1
, pp. 105-116
-
-
Williams, N.G.1
Roberts, T.M.2
-
22
-
-
2942630176
-
Locus Link
-
Pruitt KD, Maglott DR: Locus Link. 2003 [http://www.ncbi.nlm.nih.gov/LocusLink/LocRpt.cgi?l=673].
-
(2003)
-
-
Pruitt, K.D.1
Maglott, D.R.2
-
23
-
-
18444374405
-
Mutations of the BRAF gene in human cancer
-
Davies H, Bignell GR, Cox C, Stephens P, Edkins S, Clegg S, Teague J, Woffendin H, Garnett MJ, Bottomley W, Davis N, Dicks E, Ewing R, Floyd Y, Gray K, Hall S, Hawes R, Hughes J, Kosmidou V, Menzies A, Mould C, Parker A, Stevens C, Watt S, Hooper S, Wilson R, Jayatilake H, Gusterson BA, Cooper C, Shipley J, Hargrave D, Pritchard-Jones K, Maitland N, Chenevix-Trench G, Riggins GJ, Bigner DD, Palmieri G, Cossu A, Flanagan A, Nicholson A, Ho JW, Leung SY, Yuen ST, Weber BL, Seigler HF, Darrow TL, Paterson H, Marais R, Marshall CJ, Wooster R, Stratton MR, Futreal PA: Mutations of the BRAF gene in human cancer. Nature 2002, 417(6892):949-954.
-
(2002)
Nature
, vol.417
, Issue.6892
, pp. 949-954
-
-
Davies, H.1
Bignell, G.R.2
Cox, C.3
Stephens, P.4
Edkins, S.5
Clegg, S.6
Teague, J.7
Woffendin, H.8
Garnett, M.J.9
Bottomley, W.10
Davis, N.11
Dicks, E.12
Ewing, R.13
Floyd, Y.14
Gray, K.15
Hall, S.16
Hawes, R.17
Hughes, J.18
Kosmidou, V.19
Menzies, A.20
Mould, C.21
Parker, A.22
Stevens, C.23
Watt, S.24
Hooper, S.25
Wilson, R.26
Jayatilake, H.27
Gusterson, B.A.28
Cooper, C.29
Shipley, J.30
Hargrave, D.31
Pritchard-Jones, K.32
Maitland, N.33
Chenevix-Trench, G.34
Riggins, G.J.35
Bigner, D.D.36
Palmieri, G.37
Cossu, A.38
Flanagan, A.39
Nicholson, A.40
Ho, J.W.41
Leung, S.Y.42
Yuen, S.T.43
Weber, B.L.44
Seigler, H.F.45
Darrow, T.L.46
Paterson, H.47
Marais, R.48
Marshall, C.J.49
Wooster, R.50
Stratton, M.R.51
Futreal, P.A.52
more..
-
24
-
-
0037222652
-
Absence of exon 15 BRAF germline mutations in familial melanoma
-
Lang J, Boxer M, MacKie R: Absence of exon 15 BRAF germline mutations in familial melanoma. Hum Mutat 2003, 21(3):327-330.
-
(2003)
Hum. Mutat.
, vol.21
, Issue.3
, pp. 327-330
-
-
Lang, J.1
Boxer, M.2
MacKie, R.3
-
25
-
-
0038408488
-
BRAF as a melanoma susceptibility candidate gene?
-
Laud K, Kannengiesser C, Avril MF, Chompret A, Stoppa-Lyonnet D, Desjardins L, Eychene A, Demenais F, Lenoir GM, Bressac-de Paillerets B: BRAF as a melanoma susceptibility candidate gene? Cancer Res 2003, 63(12):3061-3065.
-
(2003)
Cancer Res.
, vol.63
, Issue.12
, pp. 3061-3065
-
-
Laud, K.1
Kannengiesser, C.2
Avril, M.F.3
Chompret, A.4
Stoppa-Lyonnet, D.5
Desjardins, L.6
Eychene, A.7
Demenais, F.8
Lenoir, G.M.9
Bressac-de Paillerets, B.10
-
26
-
-
0037531526
-
Exclusion of BRAFV599E as a melanoma susceptibility mutation
-
Meyer P, Klaes R, Schmitt C, Boettger MB, Garbe C: Exclusion of BRAFV599E as a melanoma susceptibility mutation. Int J Cancer 2003, 106(1):78-80.
-
(2003)
Int. J. Cancer
, vol.106
, Issue.1
, pp. 78-80
-
-
Meyer, P.1
Klaes, R.2
Schmitt, C.3
Boettger, M.B.4
Garbe, C.5
-
27
-
-
0038664387
-
BRAF mutation in papillary thyroid carcinoma
-
Cohen Y, Xing M, Mambo E, Guo Z, Wu G, Trink B, Beller U, Westra WH, Ladenson PW, Sidransky D: BRAF mutation in papillary thyroid carcinoma. J Natl Cancer Inst 2003, 95(8):625-627.
-
(2003)
J. Natl. Cancer Inst.
, vol.95
, Issue.8
, pp. 625-627
-
-
Cohen, Y.1
Xing, M.2
Mambo, E.3
Guo, Z.4
Wu, G.5
Trink, B.6
Beller, U.7
Westra, W.H.8
Ladenson, P.W.9
Sidransky, D.10
-
28
-
-
0142135475
-
BRAF mutations in papillary carcinomas of the thyroid
-
Fukushima T, Suzuki S, Mashiko M, Ohtake T, Endo Y, Takebayashi Y, Sekikawa K, Hagiwara K, Takenoshita S: BRAF mutations in papillary carcinomas of the thyroid. Oncogene 2003, 22(41):6455-6457.
-
(2003)
Oncogene
, vol.22
, Issue.41
, pp. 6455-6457
-
-
Fukushima, T.1
Suzuki, S.2
Mashiko, M.3
Ohtake, T.4
Endo, Y.5
Takebayashi, Y.6
Sekikawa, K.7
Hagiwara, K.8
Takenoshita, S.9
-
29
-
-
0037379904
-
High prevalence of BRAF mutations in thyroid cancer: Genetic evidence for constitutive activation of the RET/PTCRAS-BRAF signaling pathway in papillary thyroid carcinoma
-
Kimura ET, Nikiforova MN, Zhu Z, Knauf JA, Nikiforov YE, Fagin JA: High prevalence of BRAF mutations in thyroid cancer: genetic evidence for constitutive activation of the RET/PTCRAS-BRAF signaling pathway in papillary thyroid carcinoma. Cancer Res 2003, 63(7):1454-1457.
-
(2003)
Cancer Res.
, vol.63
, Issue.7
, pp. 1454-1457
-
-
Kimura, E.T.1
Nikiforova, M.N.2
Zhu, Z.3
Knauf, J.A.4
Nikiforov, Y.E.5
Fagin, J.A.6
-
30
-
-
0141453014
-
Clinical implication of hot spot BRAF mutation, V599E, in papillary thyroid cancers
-
Namba H, Nakashima M, Hayashi T, Hayashida N, Maeda S, Rogounovitch TI, Ohtsuru A, Saenko VA, Kanematsu T, Yamashita S: Clinical implication of hot spot BRAF mutation, V599E, in papillary thyroid cancers. J Clin Endocrinol Metab 2003, 88(9):4393-4397.
-
(2003)
J. Clin. Endocrinol. Metab.
, vol.88
, Issue.9
, pp. 4393-4397
-
-
Namba, H.1
Nakashima, M.2
Hayashi, T.3
Hayashida, N.4
Maeda, S.5
Rogounovitch, T.I.6
Ohtsuru, A.7
Saenko, V.A.8
Kanematsu, T.9
Yamashita, S.10
-
31
-
-
0041589377
-
High prevalence of BRAF gene mutation in papillary thyroid carcinomas and thyroid tumor cell lines
-
Xu X, Quiros RM, Gattuso P, Ain KB, Prinz RA: High prevalence of BRAF gene mutation in papillary thyroid carcinomas and thyroid tumor cell lines. Cancer Res 2003, 63(15):4561-4567.
-
(2003)
Cancer Res.
, vol.63
, Issue.15
, pp. 4561-4567
-
-
Xu, X.1
Quiros, R.M.2
Gattuso, P.3
Ain, K.B.4
Prinz, R.A.5
-
32
-
-
0036894746
-
BRAF and RAS mutations in human lung cancer and melanoma
-
Brose MS, Volpe P, Feldman M, Kumar M, Rishi I, Gerrero R, Einhorn E, Herlyn M, Minna J, Nicholson A, Roth JA, Albelda SM, Davies H, Cox C, Brignell G, Stephens P, Futreal PA, Wooster R, Stratton MR, Weber BL: BRAF and RAS mutations in human lung cancer and melanoma. Cancer Res 2002, 62(23):6997-7000.
-
(2002)
Cancer Res.
, vol.62
, Issue.23
, pp. 6997-7000
-
-
Brose, M.S.1
Volpe, P.2
Feldman, M.3
Kumar, M.4
Rishi, I.5
Gerrero, R.6
Einhorn, E.7
Herlyn, M.8
Minna, J.9
Nicholson, A.10
Roth, J.A.11
Albelda, S.M.12
Davies, H.13
Cox, C.14
Brignell, G.15
Stephens, P.16
Futreal, P.A.17
Wooster, R.18
Stratton, M.R.19
Weber, B.L.20
more..
-
33
-
-
0036895599
-
Missense mutations of the BRAF gene in human lung adenocarcinoma
-
Naoki K, Chen TH, Richards WG, Sugarbaker DJ, Meyerson M: Missense mutations of the BRAF gene in human lung adenocarcinoma. Cancer Res 2002, 62(23):7001-7003.
-
(2002)
Cancer Res.
, vol.62
, Issue.23
, pp. 7001-7003
-
-
Naoki, K.1
Chen, T.H.2
Richards, W.G.3
Sugarbaker, D.J.4
Meyerson, M.5
-
34
-
-
0037194728
-
Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status
-
Rajagopalan H, Bardelli A, Lengauer C, Kinzler KW, Vogelstein B, Velculescu VE: Tumorigenesis: RAF/RAS oncogenes and mismatch-repair status.Nature 2002, 418(6901):934.
-
(2002)
Nature
, vol.418
, Issue.6901
, pp. 934
-
-
Rajagopalan, H.1
Bardelli, A.2
Lengauer, C.3
Kinzler, K.W.4
Vogelstein, B.5
Velculescu, V.E.6
-
35
-
-
0141593677
-
BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair
-
Wang L, Cunningham JM, Winters JL, Guenther JC, French AJ, Boardman LA, Burgart LJ, McDonnell SK, Schaid DJ, Thibodeau SN: BRAF mutations in colon cancer are not likely attributable to defective DNA mismatch repair. Cancer Res 2003, 63(17):5209-5212.
-
(2003)
Cancer Res.
, vol.63
, Issue.17
, pp. 5209-5212
-
-
Wang, L.1
Cunningham, J.M.2
Winters, J.L.3
Guenther, J.C.4
French, A.J.5
Boardman, L.A.6
Burgart, L.J.7
McDonnell, S.K.8
Schaid, D.J.9
Thibodeau, S.N.10
-
36
-
-
0037112438
-
Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia
-
Yuen ST, Davies H, Chan TL, Ho JW, Bignell GR, Cox C, Stephens P, Edkins S, Tsui WW, Chan AS, Futreal PA, Stratton MR, Wooster R, Leung SY: Similarity of the phenotypic patterns associated with BRAF and KRAS mutations in colorectal neoplasia. Cancer Res 2002, 62(22):6451-6455.
-
(2002)
Cancer Res.
, vol.62
, Issue.22
, pp. 6451-6455
-
-
Yuen, S.T.1
Davies, H.2
Chan, T.L.3
Ho, J.W.4
Bignell, G.R.5
Cox, C.6
Stephens, P.7
Edkins, S.8
Tsui, W.W.9
Chan, A.S.10
Futreal, P.A.11
Stratton, M.R.12
Wooster, R.13
Leung, S.Y.14
-
37
-
-
0035895258
-
High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry
-
Buetow KH, Edmonson M, MacDonald R, Clifford R, Yip P, Kelley J, Little DP, Strausberg R, Koester H, Cantor CR, Braun A: High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Proc Natl Acad Sci U S A 2001, 98(2):581-584.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, Issue.2
, pp. 581-584
-
-
Buetow, K.H.1
Edmonson, M.2
MacDonald, R.3
Clifford, R.4
Yip, P.5
Kelley, J.6
Little, D.P.7
Strausberg, R.8
Koester, H.9
Cantor, C.R.10
Braun, A.11
-
38
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M, Smith NJ, Donnelly P: A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001, 68(4):978-989.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, Issue.4
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
|