-
1
-
-
0029833872
-
Hereditary nonpolyposis colorectal cancer (Lynch syndrome): An updated review
-
Lynch HT, Smyrk T. Hereditary nonpolyposis colorectal cancer (Lynch syndrome): an updated review. Cancer 1996;78:1149-67.
-
(1996)
Cancer
, vol.78
, pp. 1149-1167
-
-
Lynch, H.T.1
Smyrk, T.2
-
2
-
-
0030061148
-
Better survival rates in patients with MLH1-associated hereditary colorectal cancer
-
Sankila R, Aaltonen LA, Jarvinen HJ, Mecklin J. Better survival rates in patients with MLH1-associated hereditary colorectal cancer. Gastroenterology 1996;110:682-7.
-
(1996)
Gastroenterology
, vol.110
, pp. 682-687
-
-
Sankila, R.1
Aaltonen, L.A.2
Jarvinen, H.J.3
Mecklin, J.4
-
3
-
-
0030065387
-
Colorectal cancer, survival advantage, and hereditary nonpolyposis colorectal cancer
-
Lynch HT, Smyrk T. Colorectal cancer, survival advantage, and hereditary nonpolyposis colorectal cancer. Gastroenterology 1996;110:943-7.
-
(1996)
Gastroenterology
, vol.110
, pp. 943-947
-
-
Lynch, H.T.1
Smyrk, T.2
-
4
-
-
0017818820
-
Genetic and pathologic findings in a kindred with hereditary sarcoma breast cancer, brain tumors, leukemia, lung, laryngeal, and adrenal cortical carcinoma
-
Lynch HT, Mulcahy GM, Harris RE, Guirgis HA, Lynch JF. Genetic and pathologic findings in a kindred with hereditary sarcoma breast cancer, brain tumors, leukemia, lung, laryngeal, and adrenal cortical carcinoma. Cancer 1978;41:2055-64.
-
(1978)
Cancer
, vol.41
, pp. 2055-2064
-
-
Lynch, H.T.1
Mulcahy, G.M.2
Harris, R.E.3
Guirgis, H.A.4
Lynch, J.F.5
-
6
-
-
0025633582
-
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas and other neoplasms
-
Malkin D, Li FP, Stron LC, Fraumeni JF Jr., Nelson CE, Kim DH, et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas and other neoplasms. Science 1990;250:1233-8.
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Stron, L.C.3
Fraumeni Jr., J.F.4
Nelson, C.E.5
Kim, D.H.6
-
7
-
-
0027504088
-
Antioncogenes and human cancer
-
Knudson AG. Antioncogenes and human cancer. Proc Natl Acad Sci USA 1993;90:10914-21.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10914-10921
-
-
Knudson, A.G.1
-
8
-
-
0030239754
-
Is human patched the gatekeeper of common skin cancers?
-
Sidransky D. Is human patched the gatekeeper of common skin cancers? Nat Genet 1996;14:7-8.
-
(1996)
Nat Genet
, vol.14
, pp. 7-8
-
-
Sidransky, D.1
-
9
-
-
16044363842
-
The role of the human homologue Drosophila patched in sporadic basal cell carcinomas
-
Gailani MR, Stahle-Backdahl M, Leffell DJ, Glynn M, Zaphiropoulos PG, Pressman C, et al. The role of the human homologue Drosophila patched in sporadic basal cell carcinomas. Nat Genet 1996;14:78-81.
-
(1996)
Nat Genet
, vol.14
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
Glynn, M.4
Zaphiropoulos, P.G.5
Pressman, C.6
-
10
-
-
0030075116
-
Psychosocial consequences of DNA analysis for MEN type 2
-
Grosfeld FJM, Lips CJM, Beemer FA. Psychosocial consequences of DNA analysis for MEN type 2. Oncology 1996;10:141-6.
-
(1996)
Oncology
, vol.10
, pp. 141-146
-
-
Grosfeld, F.J.M.1
Lips, C.J.M.2
Beemer, F.A.3
-
11
-
-
0030028939
-
Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B
-
Skinner MA, DeBenedetti MK, Moley JF, Norton JA, Wells SA Jr. Medullary thyroid carcinoma in children with multiple endocrine neoplasia types 2A and 2B. J Pediatr Surg 1996;31:177-81.
-
(1996)
J Pediatr Surg
, vol.31
, pp. 177-181
-
-
Skinner, M.A.1
DeBenedetti, M.K.2
Moley, J.F.3
Norton, J.A.4
Wells Jr., S.A.5
-
12
-
-
0025326726
-
A major segment of the neurofibromatosis type 1 gene: CDNA sequence, genomic structure and point mutations
-
Cawthon RM, Weiss R, Xu G, Viskochil D, Culver M, Stevens J, et al. A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure and point mutations. Cell 1990;62:193-201.
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.M.1
Weiss, R.2
Xu, G.3
Viskochil, D.4
Culver, M.5
Stevens, J.6
-
13
-
-
0025297599
-
Type 1 neurofibromatosis gene: Identification of a large transcript disrupted in three NF1 patients
-
Wallace MR, Marchuk DA, Andersen LB, Letcher R, Odeh HM, Saulino AM, et al. Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 1990;249:181-6.
-
(1990)
Science
, vol.249
, pp. 181-186
-
-
Wallace, M.R.1
Marchuk, D.A.2
Andersen, L.B.3
Letcher, R.4
Odeh, H.M.5
Saulino, A.M.6
-
14
-
-
0029796244
-
Identification and mapping of type 1 neurofibromatosis (NF1) homologous loci
-
Cummings LM, Trent JM, Marchuk DA. Identification and mapping of type 1 neurofibromatosis (NF1) homologous loci. Cytogenet Cell Genet 1996;73:334-40.
-
(1996)
Cytogenet Cell Genet
, vol.73
, pp. 334-340
-
-
Cummings, L.M.1
Trent, J.M.2
Marchuk, D.A.3
-
15
-
-
0027979146
-
Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders
-
Shannon KM, O'Connell GA, Martin GA, Paderanga K, Olson K, Dinndorf P, et al. Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders. N Engl J Med 1994;330:597-601.
-
(1994)
N Engl J Med
, vol.330
, pp. 597-601
-
-
Shannon, K.M.1
O'Connell, G.A.2
Martin, G.A.3
Paderanga, K.4
Olson, K.5
Dinndorf, P.6
-
17
-
-
0029774092
-
Germ-line mutations in the neurofibromatosis 2 gene: Correlations with disease severity and retinal abnormalities
-
Parry DM, MacCollin MM, Kaiser-Kupfer MI, Pulaski K, Nicholson HS, Bolesta M, et al. Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities. Am J Hum Genet 1996;59:529-39.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 529-539
-
-
Parry, D.M.1
MacCollin, M.M.2
Kaiser-Kupfer, M.I.3
Pulaski, K.4
Nicholson, H.S.5
Bolesta, M.6
-
18
-
-
0029944668
-
Familial pancreatic cancer: A review
-
Lynch HT, Smyrk T, Kern SE, Hruban RH, Lightdale CJ, Lemon SJ, et al. Familial pancreatic cancer: a review. Semin Oncol 1996;23:251-75.
-
(1996)
Semin Oncol
, vol.23
, pp. 251-275
-
-
Lynch, H.T.1
Smyrk, T.2
Kern, S.E.3
Hruban, R.H.4
Lightdale, C.J.5
Lemon, S.J.6
-
19
-
-
0023807240
-
Life-style risk factors for pancreatic cancer in Louisiana: A case-control study
-
Falk RT, Pickle LW, Fontham ET, Correa P, Fraumeni JF Jr. Life-style risk factors for pancreatic cancer in Louisiana: a case-control study. Am J Epidermiol 1988;128:324-36.
-
(1988)
Am J Epidermiol
, vol.128
, pp. 324-336
-
-
Falk, R.T.1
Pickle, L.W.2
Fontham, E.T.3
Correa, P.4
Fraumeni Jr., J.F.5
-
20
-
-
0026324378
-
Reported family aggregation of pancreatic cancer within a population-based case-control study in the Francophone community in Montreal, Canada
-
Ghadirian P, Boyle P, Simard A, Baillargeon J, Maisonneuve P, Perret C. Reported family aggregation of pancreatic cancer within a population-based case-control study in the Francophone community in Montreal, Canada. Int J Pancreatol 1991;10:183-96.
-
(1991)
Int J Pancreatol
, vol.10
, pp. 183-196
-
-
Ghadirian, P.1
Boyle, P.2
Simard, A.3
Baillargeon, J.4
Maisonneuve, P.5
Perret, C.6
-
21
-
-
0028059330
-
Frequent somatic mutations and homozygous deletions of the p16(MTS1) gene in pancreatic adenocarcinoma
-
Caldas C, Hahn SA, da Costa-Luis T, Redston MS, Schutte M, Seymour AB, et al. Frequent somatic mutations and homozygous deletions of the p16(MTS1) gene in pancreatic adenocarcinoma. Nat Genet 1994;8:27-32.
-
(1994)
Nat Genet
, vol.8
, pp. 27-32
-
-
Caldas, C.1
Hahn, S.A.2
Da Costa-Luis, T.3
Redston, M.S.4
Schutte, M.5
Seymour, A.B.6
-
22
-
-
0029009926
-
Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
-
Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, et al. Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds. Nat Genet 1995;10:351-3.
-
(1995)
Nat Genet
, vol.10
, pp. 351-353
-
-
Gruis, N.A.1
Van der Velden, P.A.2
Sandkuijl, L.A.3
Prins, D.E.4
Weaver-Feldhaus, J.5
Kamb, A.6
-
24
-
-
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. N Engl J Med 1995;333:975-7.
-
(1995)
N Engl J Med
, vol.333
, pp. 975-977
-
-
Whelan, A.J.1
Bartsch, D.2
Goodfellow, P.J.3
-
25
-
-
12644253827
-
Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas
-
Goggins M, Schutte M, Lu J, Moskaluk CA, Weinstein CL, Petersen GM, et al. Germline BRCA2 gene mutations in patients with apparently sporadic pancreatic carcinomas. Cancer Res 1996;56:5360-4.
-
(1996)
Cancer Res
, vol.56
, pp. 5360-5364
-
-
Goggins, M.1
Schutte, M.2
Lu, J.3
Moskaluk, C.A.4
Weinstein, C.L.5
Petersen, G.M.6
-
26
-
-
0028328255
-
Genetics and pancreatic cancer
-
Lynch HT. Genetics and pancreatic cancer. Arch Surg 1994;129:266-8.
-
(1994)
Arch Surg
, vol.129
, pp. 266-268
-
-
Lynch, H.T.1
-
27
-
-
0026784163
-
Familial pancreatic cancer: A family study
-
Lynch HT, Fusaro L, Lynch JF. Familial pancreatic cancer: a family study. Pancreas 1992;7:511-5.
-
(1992)
Pancreas
, vol.7
, pp. 511-515
-
-
Lynch, H.T.1
Fusaro, L.2
Lynch, J.F.3
-
28
-
-
0022391090
-
Pancreatic carcinoma and hereditary nonpolyposis colorectal cancer: A family study
-
Lynch HT, Voorhees GJ, Lanspa SJ, McGreevy PS, Lynch JF. Pancreatic carcinoma and hereditary nonpolyposis colorectal cancer: a family study. Br J Cancer 1985;52:271-3.
-
(1985)
Br J Cancer
, vol.52
, pp. 271-273
-
-
Lynch, H.T.1
Voorhees, G.J.2
Lanspa, S.J.3
McGreevy, P.S.4
Lynch, J.F.5
-
29
-
-
0020557521
-
Familial atypical multiple mole-melanoma (FAMMM) syndrome: Segregation analysis
-
Lynch HT, Fusaro RM, Kimberling WJ, Lynch JF, Danes BS. Familial atypical multiple mole-melanoma (FAMMM) syndrome: segregation analysis. J Med Genet 1983;20:342-4.
-
(1983)
J Med Genet
, vol.20
, pp. 342-344
-
-
Lynch, H.T.1
Fusaro, R.M.2
Kimberling, W.J.3
Lynch, J.F.4
Danes, B.S.5
-
30
-
-
0019785626
-
Tumour spectrum in the FAMMM syndrome
-
Lynch HT, Fusaro RM, Pester J, Oosterhuis JA, Went LN, Rumke P, et al. Tumour spectrum in the FAMMM syndrome. Br J Cancer 1981;44:553-60.
-
(1981)
Br J Cancer
, vol.44
, pp. 553-560
-
-
Lynch, H.T.1
Fusaro, R.M.2
Pester, J.3
Oosterhuis, J.A.4
Went, L.N.5
Rumke, P.6
-
31
-
-
0028079835
-
The familial atypical multiple mole melanoma syndrome and its associated risk for pancreatic cancer
-
Fusaro RM, Lynch HT. The familial atypical multiple mole melanoma syndrome and its associated risk for pancreatic cancer. Int J Pancreatol 1994;16:216-21.
-
(1994)
Int J Pancreatol
, vol.16
, pp. 216-221
-
-
Fusaro, R.M.1
Lynch, H.T.2
-
32
-
-
0025284650
-
Systemic cancer and the FAMMM syndrome
-
Bergman W, Watson P, de Jong J, Lynch HT, Fusaro RM. Systemic cancer and the FAMMM syndrome. Br J Cancer 1990;61:932-6.
-
(1990)
Br J Cancer
, vol.61
, pp. 932-936
-
-
Bergman, W.1
Watson, P.2
De Jong, J.3
Lynch, H.T.4
Fusaro, R.M.5
-
33
-
-
0026471719
-
Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22
-
Canon-Albright LA, Goldgar DE, Meyer LJ, Lewis CM, Anderson DE, Fountain JW, et al. Assignment of a locus for familial melanoma, MLM, to chromosome 9p13-p22. Science 1992;258:1148-51.
-
(1992)
Science
, vol.258
, pp. 1148-1151
-
-
Canon-Albright, L.A.1
Goldgar, D.E.2
Meyer, L.J.3
Lewis, C.M.4
Anderson, D.E.5
Fountain, J.W.6
-
34
-
-
0028981766
-
Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: Correlation with phenotype
-
Chen F, Kishida T, Yao M, Hustad T, Glavac D, Dean M, et al. Germline mutations in the von Hippel-Lindau disease tumor suppressor gene: correlation with phenotype. Hum Mutat 1995;5:66-72.
-
(1995)
Hum Mutat
, vol.5
, pp. 66-72
-
-
Chen, F.1
Kishida, T.2
Yao, M.3
Hustad, T.4
Glavac, D.5
Dean, M.6
-
35
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F, Tory K, Gnarra J, Yao M, Duh F, Orcutt ML, et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 1993;260:1317-20.
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.5
Orcutt, M.L.6
-
36
-
-
9344254346
-
Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe
-
Glavac D, Neumann HPH, Wittke C, Jaenig H, Masek O, Streicher T, et al. Mutations in the VHL tumor suppressor gene and associated lesions in families with von Hippel-Lindau disease from central Europe. Hum Genet 1996;98:271-80.
-
(1996)
Hum Genet
, vol.98
, pp. 271-280
-
-
Glavac, D.1
Neumann, H.P.H.2
Wittke, C.3
Jaenig, H.4
Masek, O.5
Streicher, T.6
-
37
-
-
0022648252
-
Clinical features of colorectal carcinoma in cancer family syndrome
-
Mecklin J, Jarvinen HJ. Clinical features of colorectal carcinoma in cancer family syndrome. Dis Colon Rectum 1986;29:160-4.
-
(1986)
Dis Colon Rectum
, vol.29
, pp. 160-164
-
-
Mecklin, J.1
Jarvinen, H.J.2
-
38
-
-
0027943743
-
Pathology of hereditary nonopolyposis colorectal cancer
-
Jass JR, Smyrk TC, Stewart SM, Lane MR, Lanspa SJ, Lynch HT. Pathology of hereditary nonopolyposis colorectal cancer. Anticancer Res 1994;14:1631-4.
-
(1994)
Anticancer Res
, vol.14
, pp. 1631-1634
-
-
Jass, J.R.1
Smyrk, T.C.2
Stewart, S.M.3
Lane, M.R.4
Lanspa, S.J.5
Lynch, H.T.6
-
39
-
-
0027248156
-
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer, an updated review
-
Lynch HT, Smyrk TC, Watson P, Lanspa SJ, Lynch JF, Lynch PM, et al. Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer, an updated review. Gastroenterology 1993;104:1535-49.
-
(1993)
Gastroenterology
, vol.104
, pp. 1535-1549
-
-
Lynch, H.T.1
Smyrk, T.C.2
Watson, P.3
Lanspa, S.J.4
Lynch, J.F.5
Lynch, P.M.6
-
40
-
-
0002997195
-
Cecal, poorly differentiated adenocarcinomas, medullary-type
-
Jessurun MR, Manivel JC. Cecal, poorly differentiated adenocarcinomas, medullary-type. Mod Pathol 1992;5:43A.
-
(1992)
Mod Pathol
, vol.5
-
-
Jessurun, M.R.1
Manivel, J.C.2
-
41
-
-
0003035233
-
Histologic features of hereditary nonpolyposis colorectal carcinoma
-
Utsunomiya J, Lynch HT, editors. Tokyo: Springer-Verlag
-
Smyrk TC, Lynch HT, Watson PA, Appelman HD. Histologic features of hereditary nonpolyposis colorectal carcinoma. In: Utsunomiya J, Lynch HT, editors. Hereditary colorectal cancer. Tokyo: Springer-Verlag, 1990.
-
(1990)
Hereditary Colorectal Cancer
-
-
Smyrk, T.C.1
Lynch, H.T.2
Watson, P.A.3
Appelman, H.D.4
-
42
-
-
0025424347
-
Crohn's-like lymphoid reaction and colorectal carcinoma: A potential histologic prognosticator
-
Graham DM, Appelman HD. Crohn's-like lymphoid reaction and colorectal carcinoma: a potential histologic prognosticator. Mod Pathol 1990;3:332-5.
-
(1990)
Mod Pathol
, vol.3
, pp. 332-335
-
-
Graham, D.M.1
Appelman, H.D.2
-
43
-
-
0028276666
-
Clinical and pathological characteristics of sporadic colorectal carcinomas with DNA replication errors in microsatellite sequences
-
Kim H, Jen J, Vogelstein B, Hamilton SR. Clinical and pathological characteristics of sporadic colorectal carcinomas with DNA replication errors in microsatellite sequences. Am J Pathol 1994;145:148-56.
-
(1994)
Am J Pathol
, vol.145
, pp. 148-156
-
-
Kim, H.1
Jen, J.2
Vogelstein, B.3
Hamilton, S.R.4
-
44
-
-
0028935010
-
Biologic characterization of hereditary nonpolyposis colorectal cancer: Nuclear ploidy, AgNOR count, microvessel distribution, oncogene expression, and grade-related parameters
-
Losi L, Fante R, di Gregorio C, Aisoni ML, Lanza G, Maestri I, et al. Biologic characterization of hereditary nonpolyposis colorectal cancer: nuclear ploidy, AgNOR count, microvessel distribution, oncogene expression, and grade-related parameters. Am J Clin Pathol 1995;103:265-70.
-
(1995)
Am J Clin Pathol
, vol.103
, pp. 265-270
-
-
Losi, L.1
Fante, R.2
Di Gregorio, C.3
Aisoni, M.L.4
Lanza, G.5
Maestri, I.6
-
45
-
-
0030054532
-
Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer
-
Konishi M, Kikuchi-Yanoshita R, Tanaka K, Muraoka M, Onda A, Okumura Y, et al. Molecular nature of colon tumors in hereditary nonpolyposis colon cancer, familial polyposis, and sporadic colon cancer. Gastroenterology 1996;111:307-17.
-
(1996)
Gastroenterology
, vol.111
, pp. 307-317
-
-
Konishi, M.1
Kikuchi-Yanoshita, R.2
Tanaka, K.3
Muraoka, M.4
Onda, A.5
Okumura, Y.6
-
46
-
-
0030030036
-
Increased expression of cyclin D1 is an early event in multistage colorectal carcinogenesis
-
Arber N, Hibshoosh H, Moss SF, Sutter T, Zhang Y, Begg M, et al. Increased expression of cyclin D1 is an early event in multistage colorectal carcinogenesis. Gastroenterology 1996;110:669-74.
-
(1996)
Gastroenterology
, vol.110
, pp. 669-674
-
-
Arber, N.1
Hibshoosh, H.2
Moss, S.F.3
Sutter, T.4
Zhang, Y.5
Begg, M.6
-
47
-
-
0003628081
-
-
London: Nuffield Foundation
-
Nuffield Council on Bioethics. Genetic screening: ethical issues. London: Nuffield Foundation, 1993.
-
(1993)
Genetic Screening: Ethical Issues.
-
-
-
48
-
-
0003987981
-
-
Washington, DC: National Academy Press
-
Andrews LB, Fullerton JE, Holtzman NA, Motulsky AG. Assessing genetic risks: implications for health and social policy. Washington, DC: National Academy Press, 1994.
-
(1994)
Assessing Genetic Risks: Implications for Health and Social Policy
-
-
Andrews, L.B.1
Fullerton, J.E.2
Holtzman, N.A.3
Motulsky, A.G.4
-
49
-
-
0027983720
-
Report issued by a committee of the Health Council of the Netherlands
-
Heredity: science and society on the possibilities and limits of genetic testing and gene therpay. Report issued by a committee of the Health Council of the Netherlands. Hum Gen Ther 1994;5:37-40.
-
(1994)
Hum Gen Ther
, vol.5
, pp. 37-40
-
-
-
50
-
-
0028148836
-
Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition
-
American Society of Human Genetics. Statement of the American Society of Human Genetics on genetic testing for breast and ovarian cancer predisposition. Am J Hum Genet 1995;55:1-4.
-
(1995)
Am J Hum Genet
, vol.55
, pp. 1-4
-
-
-
51
-
-
0027945216
-
The genetic testing of children
-
Working Party of the Clinical Genetics Society. The genetic testing of children. J Med Genet 1994;31:785-97.
-
(1994)
J Med Genet
, vol.31
, pp. 785-797
-
-
-
52
-
-
0028872836
-
Points to consider: Ethical, legal and psychosocial implications of genetic testing in children and adolescents
-
American Society for Human Genetics, American College of Medical Genetics. Points to consider: ethical, legal and psychosocial implications of genetic testing in children and adolescents. Am J Hum Genet 1995;57:1233-41.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1233-1241
-
-
-
53
-
-
0029558116
-
Genetic testing, common diseases, and health service provision
-
Harper PS. Genetic testing, common diseases, and health service provision. Lancet 1995;346:1645-6.
-
(1995)
Lancet
, vol.346
, pp. 1645-1646
-
-
Harper, P.S.1
-
54
-
-
0004516701
-
-
Oslo: Ministry of Health and Social Affairs
-
Ministry of Health and Social Affairs. Biotechnology related to human beings Oslo: Ministry of Health and Social Affairs, 1993.
-
(1993)
Biotechnology Related to Human Beings
-
-
-
55
-
-
0029864134
-
Statement of the American Society of Clinical Oncology: Genetic testing for cancer susceptibility
-
American Society of Clinical Oncology. Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility. J Clin Oncol 1996;14:1730-6.
-
(1996)
J Clin Oncol
, vol.14
, pp. 1730-1736
-
-
-
56
-
-
0015519769
-
Case 25, case records of the Massachusetts General Hospital
-
Castleman B. Case 25, case records of the Massachusetts General Hospital. N Engl J Med 1972;286:1353-9.
-
(1972)
N Engl J Med
, vol.286
, pp. 1353-1359
-
-
Castleman, B.1
-
57
-
-
76949133404
-
Pedigree of a family with hereditary chronic relapsing pancreatitis
-
Comfort MW, Steinberg AG. Pedigree of a family with hereditary chronic relapsing pancreatitis. Gastroenterology 1952;21:54-63.
-
(1952)
Gastroenterology
, vol.21
, pp. 54-63
-
-
Comfort, M.W.1
Steinberg, A.G.2
-
59
-
-
0001089410
-
Hereditary pancreatitis
-
Go VLW, DiMagno EP, Gardner JD, Lebenthal E, Reber H, Scheele GA, editors. New York: Raven Press
-
Madrazo-de la Garza J, Hill ID, Lebenthal E. Hereditary pancreatitis. In: Go VLW, DiMagno EP, Gardner JD, Lebenthal E, Reber H, Scheele GA, editors. The pancreas: biology, pathobiology, and disease. New York: Raven Press, 1993:1095-101.
-
(1993)
The Pancreas: Biology, Pathobiology, and Disease
, pp. 1095-1101
-
-
Madrazo-de la Garza, J.1
Hill, I.D.2
Lebenthal, E.3
-
60
-
-
0025269723
-
Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome
-
Pipeleers-Marichal M, Somers G, Willems G, Foulis A, Imrie C, Bishop AE, et al. Gastrinomas in the duodenums of patients with multiple endocrine neoplasia type 1 and the Zollinger-Ellison syndrome. N Engl J Med 1990;322:723-7.
-
(1990)
N Engl J Med
, vol.322
, pp. 723-727
-
-
Pipeleers-Marichal, M.1
Somers, G.2
Willems, G.3
Foulis, A.4
Imrie, C.5
Bishop, A.E.6
-
61
-
-
0008965323
-
Familial colon cancer in two high risk Nebraska counties
-
San Diego
-
Lynch HT, Follett K, Shonka M, Marrero K, Fain P, Lynch J. Familial colon cancer in two high risk Nebraska counties. [abstract]. Proc AACR, San Diego, 1980.
-
(1980)
Proc AACR
-
-
Lynch, H.T.1
Follett, K.2
Shonka, M.3
Marrero, K.4
Fain, P.5
Lynch, J.6
-
62
-
-
0023204649
-
Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch Syndromes I and II)
-
Fitzgibbons RJ Jr., Lynch HT, Stanislav GV, Watson P, Lanspa SJ, Marcus JN, et al. Recognition and treatment of patients with hereditary nonpolyposis colon cancer (Lynch Syndromes I and II). Ann Surg 1987;206:289-95.
-
(1987)
Ann Surg
, vol.206
, pp. 289-295
-
-
Fitzgibbons Jr., R.J.1
Lynch, H.T.2
Stanislav, G.V.3
Watson, P.4
Lanspa, S.J.5
Marcus, J.N.6
-
63
-
-
0025963801
-
Pancreatic cancer and the familial atypical multiple mole melanoma (FAMMM) syndrome
-
Lynch HT, Fusaro RM. Pancreatic cancer and the familial atypical multiple mole melanoma (FAMMM) syndrome. Pancreas 1991;6:127-31.
-
(1991)
Pancreas
, vol.6
, pp. 127-131
-
-
Lynch, H.T.1
Fusaro, R.M.2
-
64
-
-
0025099916
-
Islet cell tumors in von Hippel-Lindau disease: Increased prevalence and relationship to the multiple endocrine neoplasias
-
Binkovitz LA, Johnson DC, Stephens DH. Islet cell tumors in von Hippel-Lindau disease: increased prevalence and relationship to the multiple endocrine neoplasias. AJR Am J Roentgenol 1990;155:501-5.
-
(1990)
AJR Am J Roentgenol
, vol.155
, pp. 501-505
-
-
Binkovitz, L.A.1
Johnson, D.C.2
Stephens, D.H.3
-
65
-
-
0028326867
-
Pancreatic lesions in von Hippel-Lindau disease: Prevalence, clinical significance, and CT findings
-
Hough DM, Stephens DH, Johnson CD, Binkovitz LA. Pancreatic lesions in von Hippel-Lindau disease: prevalence, clinical significance, and CT findings. AJR Am J Roentgenol 1994;162:1091-4.
-
(1994)
AJR Am J Roentgenol
, vol.162
, pp. 1091-1094
-
-
Hough, D.M.1
Stephens, D.H.2
Johnson, C.D.3
Binkovitz, L.A.4
-
66
-
-
1842309769
-
Autosomal dominant transmission of pancreatic cancer with diabetes and exocrine insufficiency in a large kindred
-
Burke W, Bennett RL, Schmidt R, Dellinger E, Evans JP. Autosomal dominant transmission of pancreatic cancer with diabetes and exocrine insufficiency in a large kindred [abstract 191]. Am J Hum Genet 1992;51:50.
-
(1992)
Am J Hum Genet
, vol.51
, pp. 50
-
-
Burke, W.1
Bennett, R.L.2
Schmidt, R.3
Dellinger, E.4
Evans, J.P.5
-
67
-
-
0029048904
-
Familial pancreatic adenocarcinoma: Association with diabetes and early molecular diagnosis
-
Evans JP, Burke W, Chen R, Bennett RL, Schmidt RA, Dellinger EP, et al. Familial pancreatic adenocarcinoma: association with diabetes and early molecular diagnosis. J Med Genet 1995;32:330-5.
-
(1995)
J Med Genet
, vol.32
, pp. 330-335
-
-
Evans, J.P.1
Burke, W.2
Chen, R.3
Bennett, R.L.4
Schmidt, R.A.5
Dellinger, E.P.6
|