메뉴 건너뛰기




Volumn 35, Issue 9, 1998, Pages 745-754

Predicting adaptation to presymptomatic DNA testing for late onset disorders: Who will experience distress?

(29)  DudokdeWit, A C a,c   Tibben, A a,b   Duivenvoorden, H J a   Niermeijer, M F b   Passchier, J a   Lindhout, D b   Meijers Heijboer, E J b   Frets, P G b   Lodder, L N b   Trijsburg, R W b   Zoetewij, M W b   Klijn, J G M b   Brocker Vriends A d   Van Haeringen, A d   Helderman, A T J M d   Hilhorst Hofstee, Y d   Kant, S d   Maat Kievit, J A d   Oosterwijk, J C d   Van Der Smagt, J J d   more..


Author keywords

Hereditary late onset disorders; Predicting distress; Presymptomatic dna testing

Indexed keywords

ADENOMATOUS POLYP; ADULT; ARTICLE; AVOIDANCE BEHAVIOR; BREAST CANCER; CANCER; COMPARATIVE STUDY; DISTRESS SYNDROME; DNA DETERMINATION; FEMALE; GENDER; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; HUNTINGTON CHOREA; MAJOR CLINICAL STUDY; MALE; OVARY CANCER; PATIENT COUNSELING; PRIORITY JOURNAL; RELIGION;

EID: 0006309338     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (76)

References (11)
  • 1
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 1993;72:971-83.
    • (1993) Cell , vol.72 , pp. 971-983
  • 2
    • 0026566108 scopus 로고
    • Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
    • Brook JD, McCurrach ME, Harley HG, et al. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 1992;68:799-808.
    • (1992) Cell , vol.68 , pp. 799-808
    • Brook, J.D.1    McCurrach, M.E.2    Harley, H.G.3
  • 3
    • 0028147936 scopus 로고
    • Familial Alzheimer's disease
    • Bird TD. Familial Alzheimer's disease. Ann Neurol 1994;36: 335-6.
    • (1994) Ann Neurol , vol.36 , pp. 335-336
    • Bird, T.D.1
  • 4
    • 0028067657 scopus 로고
    • Chromosome 14-encoded Alzheimer's disease: Genetic and clinicopathological description
    • Haltia M, Viitanen M, Sulkava R, et al. Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description. Ann Neurol 1994;36:362-7.
    • (1994) Ann Neurol , vol.36 , pp. 362-367
    • Haltia, M.1    Viitanen, M.2    Sulkava, R.3
  • 5
    • 0025989981 scopus 로고
    • DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type)
    • Bakker E, van Broeckhoven C, Haan J, et al. DNA diagnosis for hereditary cerebral hemorrhage with amyloidosis (Dutch type). Am J Hum Genet 1991;49:518-21.
    • (1991) Am J Hum Genet , vol.49 , pp. 518-521
    • Bakker, E.1    Van Broeckhoven, C.2    Haan, J.3
  • 6
    • 0028006563 scopus 로고
    • Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
    • Wooster R, Neuhausen SL, Mangion J, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994;265:2088-90.
    • (1994) Science , vol.265 , pp. 2088-2090
    • Wooster, R.1    Neuhausen, S.L.2    Mangion, J.3
  • 7
    • 0028113345 scopus 로고
    • A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
    • Miki Y, Swensen J, Shattuck-Eidens D, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994;266:66-71.
    • (1994) Science , vol.266 , pp. 66-71
    • Miki, Y.1    Swensen, J.2    Shattuck-Eidens, D.3
  • 8
    • 0025817880 scopus 로고
    • Identification of FAP locus genes from chromosome 5q21
    • Kinzler KW, Nilbert MC, Su LK, et al. Identification of FAP locus genes from chromosome 5q21. Science 1991;253: 661-5.
    • (1991) Science , vol.253 , pp. 661-665
    • Kinzler, K.W.1    Nilbert, M.C.2    Su, L.K.3
  • 9
    • 0025938038 scopus 로고
    • Identification and characterization of the familial adenomatous polyposis coli gene
    • Groden J, Thliveris A, Samowitz W, et al. Identification and characterization of the familial adenomatous polyposis coli gene. Cell 1991;66:589-600.
    • (1991) Cell , vol.66 , pp. 589-600
    • Groden, J.1    Thliveris, A.2    Samowitz, W.3
  • 10
    • 0028955451 scopus 로고
    • Seven new mutations in HMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis
    • Wijnen J, Vasen H, Khan PM, et al. Seven new mutations in HMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. Am J Hum Genet 1995;56: 1060-6.
    • (1995) Am J Hum Genet , vol.56 , pp. 1060-1066
    • Wijnen, J.1    Vasen, H.2    Khan, P.M.3
  • 11
    • 0028061726 scopus 로고
    • Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A
    • Wells S Jr, Chi DD, Toshima K, et al. Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Ann Surg 1994;220: 237-47.
    • (1994) Ann Surg , vol.220 , pp. 237-247
    • Wells Jr., S.1    Chi, D.D.2    Toshima, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.