-
1
-
-
77956309446
-
Genome-wide association studies of cancer
-
10.1200/JCO.2009.25.7816, 2953976, 20585100
-
Stadler ZK, Tom P, Robson ME, Weitzel JN, Kauff ND, Hurley KE, Devlin V, Gold B, Klein RJ, Offit K. Genome-wide association studies of cancer. J Clin Oncol 2010, 28:4255-4267. 10.1200/JCO.2009.25.7816, 2953976, 20585100.
-
(2010)
J Clin Oncol
, vol.28
, pp. 4255-4267
-
-
Stadler, Z.K.1
Tom, P.2
Robson, M.E.3
Weitzel, J.N.4
Kauff, N.D.5
Hurley, K.E.6
Devlin, V.7
Gold, B.8
Klein, R.J.9
Offit, K.10
-
2
-
-
77649208372
-
American society of clinical oncology policy statement update: genetic and genomic testing for cancer susceptibility
-
10.1200/JCO.2009.27.0660, 20065170
-
Robson ME, Storm CD, Weitzel J, Wollins DS, Offit K. American society of clinical oncology policy statement update: genetic and genomic testing for cancer susceptibility. J Clin Oncol 2010, 28:893-901. 10.1200/JCO.2009.27.0660, 20065170.
-
(2010)
J Clin Oncol
, vol.28
, pp. 893-901
-
-
Robson, M.E.1
Storm, C.D.2
Weitzel, J.3
Wollins, D.S.4
Offit, K.5
-
3
-
-
3543088730
-
Genetic cancer risk assessment and counseling: recommendations of the National society of genetic counselors
-
Trepanier A, Ahrens M, McKinnon W, Peters J, Stopfer J, Grumet SC, Manley S, Culver JO, Acton R, Larsen-Haidle J, Correia LA, Bennett R, Pettersen B, Ferlita TD, Costalas JW, Hunt K, Donlon S, Skrzynia C, Farrell C, Callif-Daley F, Vockley CW. Genetic cancer risk assessment and counseling: recommendations of the National society of genetic counselors. J Genet Couns 2004, 13:83-114.
-
(2004)
J Genet Couns
, vol.13
, pp. 83-114
-
-
Trepanier, A.1
Ahrens, M.2
McKinnon, W.3
Peters, J.4
Stopfer, J.5
Grumet, S.C.6
Manley, S.7
Culver, J.O.8
Acton, R.9
Larsen-Haidle, J.10
Correia, L.A.11
Bennett, R.12
Pettersen, B.13
Ferlita, T.D.14
Costalas, J.W.15
Hunt, K.16
Donlon, S.17
Skrzynia, C.18
Farrell, C.19
Callif-Daley, F.20
Vockley, C.W.21
more..
-
5
-
-
80052333832
-
Genetics, genomics and risk assessment: state of the art and future directions in the era of personalized medicine
-
Weitzel JN, Blazer KR, Mac Donald DJ, Culver OJ, Offit K. Genetics, genomics and risk assessment: state of the art and future directions in the era of personalized medicine. CA Cancer J Clin 2011, 61:327-359.
-
(2011)
CA Cancer J Clin
, vol.61
, pp. 327-359
-
-
Weitzel, J.N.1
Blazer, K.R.2
Mac Donald, D.J.3
Culver, O.J.4
Offit, K.5
-
6
-
-
0343918505
-
BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer
-
10.1056/NEJM199705153362002, 9145677
-
Couch F, DeShano ML, Blackwood MA, Calzone K, Stopfer J, Campeau L, Ganguly A, Rebbeck T, Weber BL. BRCA1 mutations in women attending clinics that evaluate the risk of breast cancer. N Engl J Med 1997, 336:1409-1415. 10.1056/NEJM199705153362002, 9145677.
-
(1997)
N Engl J Med
, vol.336
, pp. 1409-1415
-
-
Couch, F.1
DeShano, M.L.2
Blackwood, M.A.3
Calzone, K.4
Stopfer, J.5
Campeau, L.6
Ganguly, A.7
Rebbeck, T.8
Weber, B.L.9
-
7
-
-
78650197659
-
Predicting BRCA1 and BRCA2 gene mutationcarriers: comparison of PENN II model to previous study
-
10.1007/s10689-010-9348-3, 2981620, 20512419
-
Lindor NM, Johnson KJ, Harvey H, Shane Pankratz V, Domchek SM, Hunt K, Wilson M, Cathie Smith M, Couch F. Predicting BRCA1 and BRCA2 gene mutationcarriers: comparison of PENN II model to previous study. Fam Cancer 2010, 9:495-502. 10.1007/s10689-010-9348-3, 2981620, 20512419.
-
(2010)
Fam Cancer
, vol.9
, pp. 495-502
-
-
Lindor, N.M.1
Johnson, K.J.2
Harvey, H.3
Shane Pankratz, V.4
Domchek, S.M.5
Hunt, K.6
Wilson, M.7
Cathie Smith, M.8
Couch, F.9
-
8
-
-
0037087536
-
Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals
-
10.1200/JCO.20.6.1480, 11896095
-
Frank TS, Deffenbaugh AM, Reid JE, Hulick M, Ward BE, Lingenfelter B, Gumpper KL, Scholl T, Tavtigian SV, Pruss DR, Critchfield GC. Clinical characteristics of individuals with germline mutations in BRCA1 and BRCA2: analysis of 10,000 individuals. J Clin Oncol 2002, 20:1480-1490. 10.1200/JCO.20.6.1480, 11896095.
-
(2002)
J Clin Oncol
, vol.20
, pp. 1480-1490
-
-
Frank, T.S.1
Deffenbaugh, A.M.2
Reid, J.E.3
Hulick, M.4
Ward, B.E.5
Lingenfelter, B.6
Gumpper, K.L.7
Scholl, T.8
Tavtigian, S.V.9
Pruss, D.R.10
Critchfield, G.C.11
-
9
-
-
0036605379
-
BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes
-
10.1200/JCO.2002.05.121, 12039933
-
Berry DA, Iversen ES, Gudbjartsson DF, Hiller EH, Garber JE, Peshkin BN, Lerman C, Watson P, Lynch HT, Hilsenbeck SG, Rubinstein WS, Hughes KS, Parmigiani G. BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. J Clin Oncol 2002, 20:2701-2712. 10.1200/JCO.2002.05.121, 12039933.
-
(2002)
J Clin Oncol
, vol.20
, pp. 2701-2712
-
-
Berry, D.A.1
Iversen, E.S.2
Gudbjartsson, D.F.3
Hiller, E.H.4
Garber, J.E.5
Peshkin, B.N.6
Lerman, C.7
Watson, P.8
Lynch, H.T.9
Hilsenbeck, S.G.10
Rubinstein, W.S.11
Hughes, K.S.12
Parmigiani, G.13
-
10
-
-
0031029633
-
Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history
-
10.1093/jnci/89.3.227, 9017003
-
Berry DA, Parmigiani G, Sanchez J, Schildkraut J, Winer E. Probability of carrying a mutation of breast-ovarian cancer gene BRCA1 based on family history. J Natl Cancer Inst 1997, 89:227-238. 10.1093/jnci/89.3.227, 9017003.
-
(1997)
J Natl Cancer Inst
, vol.89
, pp. 227-238
-
-
Berry, D.A.1
Parmigiani, G.2
Sanchez, J.3
Schildkraut, J.4
Winer, E.5
-
11
-
-
0031917403
-
Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2
-
10.1086/301670, 1376797, 9443863
-
Parmigiani G, Berry D, Aguilar O. Determining carrier probabilities for breast cancer-susceptibility genes BRCA1 and BRCA2. Am J Hum Genet 1998, 62:145-158. 10.1086/301670, 1376797, 9443863.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 145-158
-
-
Parmigiani, G.1
Berry, D.2
Aguilar, O.3
-
12
-
-
1842680082
-
A breast cancer prediction model incorporating familial and personal risk factors
-
10.1002/sim.1668, 15057881
-
Tyrer J, Duffy SW, Cuzick J. A breast cancer prediction model incorporating familial and personal risk factors. Stat Med 2004, 23:1111-1130. 10.1002/sim.1668, 15057881.
-
(2004)
Stat Med
, vol.23
, pp. 1111-1130
-
-
Tyrer, J.1
Duffy, S.W.2
Cuzick, J.3
-
13
-
-
7944237307
-
The BOADICEA model of genetic susceptibility to breast and ovarian cancer
-
2409934, 15381934
-
Antoniou AC, Pharoah PP, Smith P, Easton DF. The BOADICEA model of genetic susceptibility to breast and ovarian cancer. Br J Cancer 2004, 91:1580-1590. 2409934, 15381934.
-
(2004)
Br J Cancer
, vol.91
, pp. 1580-1590
-
-
Antoniou, A.C.1
Pharoah, P.P.2
Smith, P.3
Easton, D.F.4
-
14
-
-
0032552239
-
Clinical findings with implications for genetic testing in families with clustering of colorectal cancer
-
10.1056/NEJM199808203390804, 9709044
-
Wijnen JT, Vasen HFA, Khan PM, Zwinderman AH, van der Klift H, Mulder A, Tops C, Møller P, Fodde R. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. N Engl J Med 1998, 339:511-518. 10.1056/NEJM199808203390804, 9709044.
-
(1998)
N Engl J Med
, vol.339
, pp. 511-518
-
-
Wijnen, J.T.1
Vasen, H.F.A.2
Khan, P.M.3
Zwinderman, A.H.4
van der Klift, H.5
Mulder, A.6
Tops, C.7
Møller, P.8
Fodde, R.9
-
15
-
-
33749066191
-
Colon cancer family registry: prediction of germline mutations and cancer risk in the Lynch syndrome
-
10.1001/jama.296.12.1479, 2538673, 17003396
-
Chen S, Wang W, Lee S, Nafa K, Lee J, Romans K, Watson P, Gruber SB, Euhus D, Kinzler KW, Jass J, Gallinger S, Lindor NM, Casey G, Ellis N, Giardiello FM, Offit K, Parmigiani G. Colon cancer family registry: prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA 2006, 296:1479-1487. 10.1001/jama.296.12.1479, 2538673, 17003396.
-
(2006)
JAMA
, vol.296
, pp. 1479-1487
-
-
Chen, S.1
Wang, W.2
Lee, S.3
Nafa, K.4
Lee, J.5
Romans, K.6
Watson, P.7
Gruber, S.B.8
Euhus, D.9
Kinzler, K.W.10
Jass, J.11
Gallinger, S.12
Lindor, N.M.13
Casey, G.14
Ellis, N.15
Giardiello, F.M.16
Offit, K.17
Parmigiani, G.18
-
16
-
-
33745658837
-
Identification and survival of carriers of mutations in DNA mismatchrepair genes in colon cancer
-
10.1056/NEJMoa053493, 16807412
-
Barnetson RA, Tenesa A, Farrington SM, Nicholl ID, Cetnarskyj R, Porteous ME, Campbell H, Dunlop MG. Identification and survival of carriers of mutations in DNA mismatchrepair genes in colon cancer. N Engl J Med 2006, 354:2751-2763. 10.1056/NEJMoa053493, 16807412.
-
(2006)
N Engl J Med
, vol.354
, pp. 2751-2763
-
-
Barnetson, R.A.1
Tenesa, A.2
Farrington, S.M.3
Nicholl, I.D.4
Cetnarskyj, R.5
Porteous, M.E.6
Campbell, H.7
Dunlop, M.G.8
-
17
-
-
78650513224
-
The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history
-
10.1053/j.gastro.2010.08.021, 3125673, 20727894
-
Kastrinos F, Steyerberg EW, Mercado R, Balmaña J, Holter S, Gallinger S, Siegmund KD, Church JM, Jenkins MA, Lindor NM, Thibodeau SN, Burbidge LA, Wenstrup RJ, Syngal S. The PREMM(1,2,6) model predicts risk of MLH1, MSH2, and MSH6 germline mutations based on cancer history. Gastroenterology 2011, 140:73-81. 10.1053/j.gastro.2010.08.021, 3125673, 20727894.
-
(2011)
Gastroenterology
, vol.140
, pp. 73-81
-
-
Kastrinos, F.1
Steyerberg, E.W.2
Mercado, R.3
Balmaña, J.4
Holter, S.5
Gallinger, S.6
Siegmund, K.D.7
Church, J.M.8
Jenkins, M.A.9
Lindor, N.M.10
Thibodeau, S.N.11
Burbidge, L.A.12
Wenstrup, R.J.13
Syngal, S.14
-
18
-
-
0033063711
-
New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International collaborative group on HNPCC
-
10.1016/S0016-5085(99)70510-X, 10348829
-
Vasen HF, Watson P, Mecklin JP, Lynch HT. New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International collaborative group on HNPCC. Gastroenterology 1999, 116:1453-1456. 10.1016/S0016-5085(99)70510-X, 10348829.
-
(1999)
Gastroenterology
, vol.116
, pp. 1453-1456
-
-
Vasen, H.F.1
Watson, P.2
Mecklin, J.P.3
Lynch, H.T.4
-
19
-
-
10744233937
-
Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
-
10.1093/jnci/djh034, 2933058, 14970275
-
Umar A, Boland CR, Terdiman JP, Syngal S, de la Chapelle A, Rüschoff J, Fishel R, Lindor NM, Burgart LJ, Hamelin R, Hamilton SR, Hiatt RA, Jass J, Lindblom A, Lynch HT, Peltomaki P, Ramsey SD, Rodriguez-Bigas MA, Vasen HF, Hawk ET, Barrett JC, Freedman AN, Srivastava S. Revised Bethesda guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 2004, 96:261-268. 10.1093/jnci/djh034, 2933058, 14970275.
-
(2004)
J Natl Cancer Inst
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
Syngal, S.4
de la Chapelle, A.5
Rüschoff, J.6
Fishel, R.7
Lindor, N.M.8
Burgart, L.J.9
Hamelin, R.10
Hamilton, S.R.11
Hiatt, R.A.12
Jass, J.13
Lindblom, A.14
Lynch, H.T.15
Peltomaki, P.16
Ramsey, S.D.17
Rodriguez-Bigas, M.A.18
Vasen, H.F.19
Hawk, E.T.20
Barrett, J.C.21
Freedman, A.N.22
Srivastava, S.23
more..
-
20
-
-
0014587529
-
Soft tissue sarcomas, breast cancer and other neoplasms: a familial syndrome?
-
10.7326/0003-4819-71-4-747, 5360287
-
Li PP, Fraumeni JF. Soft tissue sarcomas, breast cancer and other neoplasms: a familial syndrome?. Ann Int Med 1969, 71:747-752. 10.7326/0003-4819-71-4-747, 5360287.
-
(1969)
Ann Int Med
, vol.71
, pp. 747-752
-
-
Li, P.P.1
Fraumeni, J.F.2
-
21
-
-
0034071085
-
P53 germline mutations in childhood cancers and cancer risk for carrier individuals
-
2363254, 10864200
-
Chompret A, Brugieres L, Ronsin M, Gardes M, Dessarps-Freichey F, Abel A, Hua D, Ligot L, Dondon MG, Bressac-de Paillerets B, Frébourg T, Lemerle J, Bonaïti-Pellié C, Feunteun J. P53 germline mutations in childhood cancers and cancer risk for carrier individuals. Br J Cancer 2000, 82:1932-1937. 2363254, 10864200.
-
(2000)
Br J Cancer
, vol.82
, pp. 1932-1937
-
-
Chompret, A.1
Brugieres, L.2
Ronsin, M.3
Gardes, M.4
Dessarps-Freichey, F.5
Abel, A.6
Hua, D.7
Ligot, L.8
Dondon, M.G.9
Bressac-de Paillerets, B.10
Frébourg, T.11
Lemerle, J.12
Bonaïti-Pellié, C.13
Feunteun, J.14
-
22
-
-
0033738748
-
Will the real Cowden syndrome please stand up: revised diagnostic criteria
-
10.1136/jmg.37.11.828, 1734465, 11073535
-
Eng C. Will the real Cowden syndrome please stand up: revised diagnostic criteria. J Med Genet 2000, 37:828-830. 10.1136/jmg.37.11.828, 1734465, 11073535.
-
(2000)
J Med Genet
, vol.37
, pp. 828-830
-
-
Eng, C.1
-
23
-
-
78650908302
-
A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands
-
10.1016/j.ajhg.2010.11.013, 3014373, 21194675
-
Tan MH, Mester J, Peterson C, Yang Y, Chen JL, Rybicki LA, Milas K, Pederson H, Remzi B, Orloff MS, Eng C. A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands. Am J Hum Genet 2011, 88:42-56. 10.1016/j.ajhg.2010.11.013, 3014373, 21194675.
-
(2011)
Am J Hum Genet
, vol.88
, pp. 42-56
-
-
Tan, M.H.1
Mester, J.2
Peterson, C.3
Yang, Y.4
Chen, J.L.5
Rybicki, L.A.6
Milas, K.7
Pederson, H.8
Remzi, B.9
Orloff, M.S.10
Eng, C.11
-
24
-
-
76549103663
-
Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO
-
10.1158/0008-5472.CAN-09-2653, 2947347, 20068151
-
Wang W, Niendorf KB, Patel D, Blackford A, Marroni F, Sober AJ, Parmigiani G, Tsao H. Estimating CDKN2A carrier probability and personalizing cancer risk assessments in hereditary melanoma using MelaPRO. Cancer Res 2010, 70:552-559. 10.1158/0008-5472.CAN-09-2653, 2947347, 20068151.
-
(2010)
Cancer Res
, vol.70
, pp. 552-559
-
-
Wang, W.1
Niendorf, K.B.2
Patel, D.3
Blackford, A.4
Marroni, F.5
Sober, A.J.6
Parmigiani, G.7
Tsao, H.8
-
25
-
-
78650801916
-
Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population
-
10.1158/1940-6207.CAPR-10-0262, 3793254, 21088223
-
Dinh TA, Rosner BI, Atwood JC, Boland CR, Syngal S, Vasen HF, Gruber SB, Burt RW. Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila) 2011, 4:9-22. 10.1158/1940-6207.CAPR-10-0262, 3793254, 21088223.
-
(2011)
Cancer Prev Res (Phila)
, vol.4
, pp. 9-22
-
-
Dinh, T.A.1
Rosner, B.I.2
Atwood, J.C.3
Boland, C.R.4
Syngal, S.5
Vasen, H.F.6
Gruber, S.B.7
Burt, R.W.8
-
26
-
-
77957967823
-
Expanding the criteria for BRCA mutation testing in breast cancer survivors
-
10.1200/JCO.2010.28.0719, 20733129
-
Kwon JS, Gutierrez-Barrera AM, Young D, Sun CC, Daniels MS, Lu KH, Arun B. Expanding the criteria for BRCA mutation testing in breast cancer survivors. J Clin Oncol 2010, 28:4214-4220. 10.1200/JCO.2010.28.0719, 20733129.
-
(2010)
J Clin Oncol
, vol.28
, pp. 4214-4220
-
-
Kwon, J.S.1
Gutierrez-Barrera, A.M.2
Young, D.3
Sun, C.C.4
Daniels, M.S.5
Lu, K.H.6
Arun, B.7
-
27
-
-
84860181053
-
-
Fort Washington, PA: National Comprehensive Cancer Network, National Comprehensive Cancer Network
-
National Comprehensive Cancer Network NCCN practice guidelines V.1.2013: genetic/familial high-risk assessment: breast and ovarian 2013, Fort Washington, PA: National Comprehensive Cancer Network, http://www.nccn.org, National Comprehensive Cancer Network.
-
(2013)
NCCN practice guidelines V.1.2013: genetic/familial high-risk assessment: breast and ovarian
-
-
-
28
-
-
84887613307
-
-
Fort Washington, PA: National Comprehensive Cancer Network, National Comprehensive Cancer Network
-
National Comprehensive Cancer Network NCCN practice guidelines V.2.2012: colorectal cancer screening 2012, Fort Washington, PA: National Comprehensive Cancer Network, http://www.nccn.org, National Comprehensive Cancer Network.
-
(2012)
NCCN practice guidelines V.2.2012: colorectal cancer screening
-
-
-
29
-
-
1242292336
-
Referral for cancer genetics consultation: a review and compilation of risk assessment criteria
-
10.1136/jmg.2003.010918, 1735676, 14757853
-
Hampel H, Sweet K, Westman JA, Offit K, Eng C. Referral for cancer genetics consultation: a review and compilation of risk assessment criteria. J Med Genet 2004, 41:81-91. 10.1136/jmg.2003.010918, 1735676, 14757853.
-
(2004)
J Med Genet
, vol.41
, pp. 81-91
-
-
Hampel, H.1
Sweet, K.2
Westman, J.A.3
Offit, K.4
Eng, C.5
-
30
-
-
0024801278
-
Projecting individualized probabilities of developing breast cancer for white females who are being examined annually
-
10.1093/jnci/81.24.1879, 2593165
-
Gail MH, Brinton LA, Byar DP, Corle DK, Green SB, Schairer C, Mulvihill JJ. Projecting individualized probabilities of developing breast cancer for white females who are being examined annually. J Natl Cancer Inst 1989, 81:1879-1886. 10.1093/jnci/81.24.1879, 2593165.
-
(1989)
J Natl Cancer Inst
, vol.81
, pp. 1879-1886
-
-
Gail, M.H.1
Brinton, L.A.2
Byar, D.P.3
Corle, D.K.4
Green, S.B.5
Schairer, C.6
Mulvihill, J.J.7
-
31
-
-
0027979310
-
Autosomal dominant inheritance of earlyonset breast cancer: implications for risk prediction
-
10.1002/1097-0142(19940201)73:3<643::AID-CNCR2820730323>3.0.CO;2-5, 8299086
-
Claus EB, Risch N, Thompson WD. Autosomal dominant inheritance of earlyonset breast cancer: implications for risk prediction. Cancer 1994, 73:643-651. 10.1002/1097-0142(19940201)73:3<643::AID-CNCR2820730323>3.0.CO;2-5, 8299086.
-
(1994)
Cancer
, vol.73
, pp. 643-651
-
-
Claus, E.B.1
Risch, N.2
Thompson, W.D.3
-
32
-
-
84855638083
-
-
National Cancer Institute (NCI)
-
National Cancer Institute (NCI) Risk factor monitoring and methods http://appliedresearch.cancer.gov/about/rfmmb/research.html, National Cancer Institute (NCI).
-
Risk factor monitoring and methods
-
-
-
33
-
-
77951585057
-
Architecture of inherited susceptibility to common cancer
-
Fletcher O, Houlston RS. Architecture of inherited susceptibility to common cancer. Nature Rev Cancer 2010, 10:353-361.
-
(2010)
Nature Rev Cancer
, vol.10
, pp. 353-361
-
-
Fletcher, O.1
Houlston, R.S.2
-
35
-
-
42549109101
-
Genetic counseling: an indispensable step in the genetic testing process
-
2793969, 20856787
-
Garber J, Zon R, Weitzel J. Genetic counseling: an indispensable step in the genetic testing process. J Oncol Pract 2008, 4(2):96-98. 2793969, 20856787.
-
(2008)
J Oncol Pract
, vol.4
, Issue.2
, pp. 96-98
-
-
Garber, J.1
Zon, R.2
Weitzel, J.3
-
36
-
-
0003939114
-
-
Cambridge, UK: Cambridge University Press, 3
-
Hodgson SV, Foulkes WD, Eng C, Maher ER. A practical guide to human cancer genetics 2007, Cambridge, UK: Cambridge University Press, 3.
-
(2007)
A practical guide to human cancer genetics
-
-
Hodgson, S.V.1
Foulkes, W.D.2
Eng, C.3
Maher, E.R.4
-
37
-
-
84880535720
-
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing
-
10.1038/gim.2013.73, 23788249
-
Green RC, Berg JS, Grody WW, Kalia SS, Korf BR, Martin CL, McGuire AL, Nussbaum RL, O'Daniel JM, Ormond KE, Rehm HL, Watson MS, Williams MS, Biesecker LG. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing. Genet Med 2013, 15(7):565-574. 10.1038/gim.2013.73, 23788249.
-
(2013)
Genet Med
, vol.15
, Issue.7
, pp. 565-574
-
-
Green, R.C.1
Berg, J.S.2
Grody, W.W.3
Kalia, S.S.4
Korf, B.R.5
Martin, C.L.6
McGuire, A.L.7
Nussbaum, R.L.8
O'Daniel, J.M.9
Ormond, K.E.10
Rehm, H.L.11
Watson, M.S.12
Williams, M.S.13
Biesecker, L.G.14
-
38
-
-
84887613848
-
-
Rio de Janeiro, Brazil: Coordenação de Educação (CEDC), Ministério da Saúde. Instituto Nacional de Câncer (INCA)
-
Ministério da Saúde. Instituto Nacional de Câncer (INCA) Rede nacional de câncer familial: manual operacional 2009, Rio de Janeiro, Brazil: Coordenação de Educação (CEDC), Ministério da Saúde. Instituto Nacional de Câncer (INCA).
-
(2009)
Rede nacional de câncer familial: manual operacional
-
-
|