-
1
-
-
23444445336
-
Statement on use of DNA testing for presymptomatic identification of cancer risk
-
National Advisory Council for Human Genome Research: Statement on use of DNA testing for presymptomatic identification of cancer risk. JAMA 271:785, 1994
-
(1994)
JAMA
, vol.271
, pp. 785
-
-
-
2
-
-
0028148836
-
Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition
-
Statement of The American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition. Am J Hum Genet 55:i-iv, 1994
-
(1994)
Am J Hum Genet
, vol.55
-
-
-
3
-
-
0029089259
-
Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspective
-
Marra G, Boland CR: Hereditary nonpolyposis colorectal cancer: The syndrome, the genes, and historical perspective. J Natl Cancer Inst 87:1114-1125, 1995
-
(1995)
J Natl Cancer Inst
, vol.87
, pp. 1114-1125
-
-
Marra, G.1
Boland, C.R.2
-
4
-
-
0028108802
-
Mismatch repair genes on chromosome 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage
-
Nystrom-Lahti M, Parsons R, Sistonen P, et al: Mismatch repair genes on chromosome 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage. Am J Hum Genet 55:659-665, 1994
-
(1994)
Am J Hum Genet
, vol.55
, pp. 659-665
-
-
Nystrom-Lahti, M.1
Parsons, R.2
Sistonen, P.3
-
5
-
-
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, Simar J, et al: 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
-
(1995)
JAMA
, vol.273
, pp. 535-541
-
-
Shattuck-Eidens, D.1
McClure, M.2
Simar, J.3
-
6
-
-
0028814530
-
Assessment and counseling for women with a family history of breast cancer
-
Hoskins KF, Stopfer JE, Calzone KA, et al: Assessment and counseling for women with a family history of breast cancer. JAMA 273:577-585, 1995
-
(1995)
JAMA
, vol.273
, pp. 577-585
-
-
Hoskins, K.F.1
Stopfer, J.E.2
Calzone, K.A.3
-
7
-
-
13344260688
-
Germ-line BRCA1 mutations in Jewish and non-Jewish women with early onset breast cancer
-
FitzGerald MG, MacDonald DJ, Krainer M, 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
-
(1996)
N Engl J Med
, vol.334
, pp. 143-149
-
-
FitzGerald, M.G.1
MacDonald, D.J.2
Krainer, M.3
-
8
-
-
0006713602
-
Identification of the breast cancer gene BRCA2
-
Wooster R, Bignell G, Lancaster J, et al: Identification of the breast cancer gene BRCA2. Nature 378:789-791, 1995
-
(1995)
Nature
, vol.378
, pp. 789-791
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
-
9
-
-
0028061726
-
Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
-
Wells SA, Chi DD, Toshima K, et al: Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Ann Surgery 220:237-250, 1994
-
(1994)
Ann Surgery
, vol.220
, pp. 237-250
-
-
Wells, S.A.1
Chi, D.D.2
Toshima, K.3
-
10
-
-
0023832168
-
Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene
-
Wiggs J, Nordenskjold M, Yandell D, et al: Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene. New Engl J Med 318:151-157, 1988
-
(1988)
New Engl J Med
, vol.318
, pp. 151-157
-
-
Wiggs, J.1
Nordenskjold, M.2
Yandell, D.3
-
11
-
-
0027763498
-
Molecular diagnosis of familial adenomatous polyposis
-
Powell S, Petersen G, Krush AJ, et al: Molecular diagnosis of familial adenomatous polyposis. New Engl J Med 329:1982-1987, 1993
-
(1993)
New Engl J Med
, vol.329
, pp. 1982-1987
-
-
Powell, S.1
Petersen, G.2
Krush, A.J.3
-
12
-
-
0029102927
-
A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor suppressor gene
-
Whelan AJ, Bartsch D, Goodfellow PJ: A familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor suppressor gene. New Engl J Med 333:975-977, 1995
-
(1995)
New Engl J Med
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
13
-
-
0027956481
-
Quantitating familial cancer risk: A resource for clinical oncologists
-
Offit K, Brown K: Quantitating familial cancer risk: A resource for clinical oncologists. J Clin Oncol 12:1724-1736, 1994
-
(1994)
J Clin Oncol
, vol.12
, pp. 1724-1736
-
-
Offit, K.1
Brown, K.2
-
14
-
-
0029131977
-
Certificates of confidentiality: A valuable tool for protecting genetic data
-
Earley CL, Strong LC: Certificates of confidentiality: A valuable tool for protecting genetic data. Am J Hum Genet 57:727-731, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 727-731
-
-
Earley, C.L.1
Strong, L.C.2
-
15
-
-
1542427506
-
-
Bethesda, MD, American College of Medical Genetics
-
American College of Medical Genetics: Standards and Guidelines: Clinical Laboratory Genetics. Bethesda, MD, American College of Medical Genetics, 1993
-
(1993)
Standards and Guidelines: Clinical Laboratory Genetics
-
-
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