메뉴 건너뛰기




Volumn 170, Issue 3, 2011, Pages 285-294

Educational paper : Screening in cancer predisposition syndromes: Guidelines for the general pediatrician

Author keywords

Beckwith Wiedemann syndrome; Cancer predisposition; Genetic testing; Li Fraumeni syndrome; Rhabdoid tumor; Von Hippel Lindau

Indexed keywords

ANTINEOPLASTIC AGENT;

EID: 79954449180     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-010-1377-2     Document Type: Review
Times cited : (57)

References (70)
  • 1
    • 0036274254 scopus 로고    scopus 로고
    • Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: A role for laparoscopic and cortical-sparing surgery
    • 12049539 10.1001/archsurg.137.6.682
    • M Baghai GB Thompson WF Young Jr, et al. 2002 Pheochromocytomas and paragangliomas in von Hippel-Lindau disease: a role for laparoscopic and cortical-sparing surgery Arch Surg 137 682 688 12049539 10.1001/archsurg.137.6. 682
    • (2002) Arch Surg , vol.137 , pp. 682-688
    • Baghai, M.1    Thompson, G.B.2    Young Jr., W.F.3
  • 3
    • 38049050719 scopus 로고    scopus 로고
    • The molecular genetics of adrenocortical carcinoma
    • 17934868 10.1007/s11154-007-9057-x
    • FM Barlaskar GD Hammer 2007 The molecular genetics of adrenocortical carcinoma Rev Endocr Metab Disord 8 343 348 17934868 10.1007/s11154-007-9057-x
    • (2007) Rev Endocr Metab Disord , vol.8 , pp. 343-348
    • Barlaskar, F.M.1    Hammer, G.D.2
  • 4
    • 0031915657 scopus 로고    scopus 로고
    • Children at increased risk for Wilms tumor: Monitoring issues
    • DOI 10.1016/S0022-3476(98)70001-0
    • JB Beckwith 1998 Children at increased risk for Wilms tumor: monitoring issues J Pediatr 132 377 379 9544882 1:STN:280:DyaK1c3gsVCnsQ%3D%3D 10.1016/S0022-3476(98)70001-0 (Pubitemid 28180231)
    • (1998) Journal of Pediatrics , vol.132 , Issue.3 , pp. 377-379
    • Beckwith, J.B.1
  • 6
    • 9744222638 scopus 로고    scopus 로고
    • Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)
    • DOI 10.1016/j.jpeds.2004.08.007, PII S0022347604007206
    • J Bliek C Gicquel S Maas, et al. 2004 Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS) J Pediatr 145 796 799 15580204 10.1016/j.jpeds.2004.08.007 (Pubitemid 39586619)
    • (2004) Journal of Pediatrics , vol.145 , Issue.6 , pp. 796-799
    • Bliek, J.1    Gicquel, C.2    Maas, S.3    Gaston, V.4    Le Bouc, Y.5    Mannens, M.6
  • 10
    • 52449103743 scopus 로고    scopus 로고
    • Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis
    • 18647326 1:CAS:528:DC%2BD1cXhsVyms7zI 10.1111/j.1399-0004.2008.01060.x
    • C Boyd MJ Smith L Kluwe, et al. 2008 Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis Clin Genet 74 358 366 18647326 1:CAS:528:DC%2BD1cXhsVyms7zI 10.1111/j.1399-0004.2008.01060.x
    • (2008) Clin Genet , vol.74 , pp. 358-366
    • Boyd, C.1    Smith, M.J.2    Kluwe, L.3
  • 11
    • 78649683466 scopus 로고    scopus 로고
    • Clincopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system
    • 10.1002/pbc.22757 20848638
    • CS Bruggers SB Bleyl T Pysher, et al. 2010 Clincopathologic comparison of familial versus sporadic atypical teratoid/rhabdoid tumors (AT/RT) of the central nervous system Pediatr Blood Cancer 10.1002/pbc.22757 20848638
    • (2010) Pediatr Blood Cancer
    • Bruggers, C.S.1    Bleyl, S.B.2    Pysher, T.3
  • 12
    • 72249110256 scopus 로고    scopus 로고
    • How should the patient with multiple endocrine neoplasia type 1 (MEN 1) be followed?
    • 19552677 10.1111/j.1365-2265.2009.03662.x
    • J Burgess 2010 How should the patient with multiple endocrine neoplasia type 1 (MEN 1) be followed? Clin Endocrinol Oxf 72 13 16 19552677 10.1111/j.1365-2265.2009.03662.x
    • (2010) Clin Endocrinol Oxf , vol.72 , pp. 13-16
    • Burgess, J.1
  • 13
    • 33748051060 scopus 로고    scopus 로고
    • Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy
    • DOI 10.1002/(SICI)1096-911X(199903)32:3<196::AID-MPO6>3.0.CO;2-9
    • PL Choyke MJ Siegel AW Craft, et al. 1999 Screening for Wilms tumor in children with Beckwith-Wiedemann syndrome or idiopathic hemihypertrophy Med Pediatr Oncol 32 196 200 10064187 1:STN:280:DyaK1M7mtF2msg%3D%3D 10.1002/(SICI)1096-911X(199903)32:3<196::AID-MPO6>3.0.CO;2-9 (Pubitemid 29095979)
    • (1999) Medical and Pediatric Oncology , vol.32 , Issue.3 , pp. 196-200
    • Choyke, P.L.1    Siegel, M.J.2    Craft, A.W.3    Green, D.M.4    DeBaun, M.R.5
  • 14
    • 0042834211 scopus 로고    scopus 로고
    • Serum α-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia
    • DOI 10.1067/S0022-3476(03)00306-8
    • CL Clericuzio E Chen DE McNeil, et al. 2003 Serum alpha-fetoprotein screening for hepatoblastoma in children with Beckwith-Wiedemann syndrome or isolated hemihyperplasia J Pediatr 143 270 272 12970646 10.1067/S0022-3476(03) 00306-8 (Pubitemid 37082965)
    • (2003) Journal of Pediatrics , vol.143 , Issue.2 , pp. 270-272
    • Clericuzio, C.L.1    Chen, E.2    McNeil, D.E.3    O'Connor, T.4    Zackai, E.H.5    Medne, L.6    Tomlinson, G.7    DeBaun, M.8
  • 15
    • 53949095425 scopus 로고    scopus 로고
    • The von Hippel-Lindau gene: Turning discovery into therapy
    • 18800388 1:CAS:528:DC%2BD1cXht1GqsrjK 10.1002/cncr.23645
    • PE Clark MS Cookson 2008 The von Hippel-Lindau gene: turning discovery into therapy Cancer 113 1768 1778 18800388 1:CAS:528:DC%2BD1cXht1GqsrjK 10.1002/cncr.23645
    • (2008) Cancer , vol.113 , pp. 1768-1778
    • Clark, P.E.1    Cookson, M.S.2
  • 16
    • 55049100981 scopus 로고    scopus 로고
    • Familial and hereditary renal cancer syndromes
    • 18992610 10.1016/j.ucl.2008.07.014
    • JA Coleman 2008 Familial and hereditary renal cancer syndromes Urol Clin North Am 35 563 572 18992610 10.1016/j.ucl.2008.07.014
    • (2008) Urol Clin North Am , vol.35 , pp. 563-572
    • Coleman, J.A.1
  • 18
    • 78649675614 scopus 로고    scopus 로고
    • Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors
    • 21108436 10.1002/pbc.22831
    • KW Eaton LS Tooke LM Wainwright, et al. 2011 Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors Pediatr Blood Cancer 56 1 7 15 21108436 10.1002/pbc.22831
    • (2011) Pediatr Blood Cancer , vol.56 , Issue.1 , pp. 7-15
    • Eaton, K.W.1    Tooke, L.S.2    Wainwright, L.M.3
  • 20
    • 77249085667 scopus 로고    scopus 로고
    • Childhood predictive genetic testing for Li-Fraumeni syndrome
    • 19404774 1:STN:280:DC%2BC3c7gvFeiug%3D%3D 10.1007/s10689-009-9245-9
    • DG Evans P Lunt T Clancy R Eeles 2010 Childhood predictive genetic testing for Li-Fraumeni syndrome Fam Cancer 9 65 69 19404774 1:STN:280:DC%2BC3c7gvFeiug%3D%3D 10.1007/s10689-009-9245-9
    • (2010) Fam Cancer , vol.9 , pp. 65-69
    • Evans, D.G.1    Lunt, P.2    Clancy, T.3    Eeles, R.4
  • 22
    • 77953957405 scopus 로고    scopus 로고
    • The neurofibromatoses
    • 20308235 10.1136/jnnp.2010.206532
    • RE Ferner 2010 The neurofibromatoses Pract Neurol 10 82 93 20308235 10.1136/jnnp.2010.206532
    • (2010) Pract Neurol , vol.10 , pp. 82-93
    • Ferner, R.E.1
  • 23
    • 34147123158 scopus 로고    scopus 로고
    • Inherited cancer susceptibility syndromes in paediatric practice
    • DOI 10.1111/j.1440-1754.2007.01027.x
    • M Field S Shanley J Kirk 2007 Inherited cancer susceptibility syndromes in paediatric practice J Paediatr Child Health 43 219 229 17444822 10.1111/j.1440-1754.2007.01027.x (Pubitemid 46570079)
    • (2007) Journal of Paediatrics and Child Health , vol.43 , Issue.4 , pp. 219-229
    • Field, M.1    Shanley, S.2    Kirk, J.3
  • 26
    • 0032475876 scopus 로고    scopus 로고
    • Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review
    • DOI 10.1002/(SICI)1096-8628(19981002)79:4<274::AID-AJMG8>3.0.CO;2-M
    • HE Hoyme LH Seaver KL Jones, et al. 1998 Isolated hemihyperplasia (hemihypertrophy): report of a prospective multicenter study of the incidence of neoplasia and review Am J Med Genet 79 274 278 9781907 1:STN:280: DyaK1cvltlWlug%3D%3D 10.1002/(SICI)1096-8628(19981002)79:4<274::AID- AJMG8>3.0.CO;2-M (Pubitemid 28447108)
    • (1998) American Journal of Medical Genetics , vol.79 , Issue.4 , pp. 274-278
    • Hoyme, H.E.1    Seaver, L.H.2    Jones, K.L.3    Procopio, F.4    Crooks, W.5    Feingold, M.6
  • 28
    • 0345269984 scopus 로고    scopus 로고
    • Germline p53 mutations in a cohort with childhood sarcoma: Sex differences in cancer risk
    • DOI 10.1086/374567
    • SJ Hwang G Lozano CI Amos LC Strong 2003 Germline p53 mutations in a cohort with childhood sarcoma: sex differences in cancer risk Am J Hum Genet 72 975 983 12610779 1:CAS:528:DC%2BD3sXivFWgurs%3D 10.1086/374567 (Pubitemid 36403315)
    • (2003) American Journal of Human Genetics , vol.72 , Issue.4 , pp. 975-983
    • Hwang, S.-J.1    Lozano, G.2    Amos, C.I.3    Strong, L.C.4
  • 30
    • 33747137225 scopus 로고    scopus 로고
    • Time trends of cancer incidence in European children (1978-1997): Report from the Automated Childhood Cancer Information System project
    • DOI 10.1016/j.ejca.2006.05.014, PII S0959804906004709, Cancer in Children and Adolescents in Europe
    • P Kaatsch E Steliarova-Foucher E Crocetti, et al. 2006 Time trends of cancer incidence in European children (1978-1997): report from the automated childhood cancer information system project Eur J Cancer 42 1961 1971 16919764 10.1016/j.ejca.2006.05.014 (Pubitemid 44224058)
    • (2006) European Journal of Cancer , vol.42 , Issue.13 , pp. 1961-1971
    • Kaatsch, P.1    Steliarova-Foucher, E.2    Crocetti, E.3    Magnani, C.4    Spix, C.5    Zambon, P.6
  • 31
    • 0037102268 scopus 로고    scopus 로고
    • Treatment of unresectable and metastatic hepatoblastoma: A pediatric oncology group phase II study
    • 12177104 10.1200/JCO.2002.07.400
    • HM Katzenstein WB London E Douglass, et al. 2002 Treatment of unresectable and metastatic hepatoblastoma: a pediatric oncology group phase II study J Clin Oncol 20 3438 3444 12177104 10.1200/JCO.2002.07.400
    • (2002) J Clin Oncol , vol.20 , pp. 3438-3444
    • Katzenstein, H.M.1    London, W.B.2    Douglass, E.3
  • 32
    • 16244373064 scopus 로고    scopus 로고
    • Tumors of the endolymphatic sac in patients with von Hippel-Lindau disease: Implications for their natural history, diagnosis, and treatment
    • HJ Kim JA Butman C Brewer, et al. 2005 Tumors of the endolymphatic sac in patients with von Hippel-Lindau disease: implications for their natural history, diagnosis and treatment J Neurosurg 102 503 512 15796386 10.3171/jns.2005.102.3.0503 (Pubitemid 43194043)
    • (2005) Journal of Neurosurgery , vol.102 , Issue.3 , pp. 503-512
    • Kim, H.J.1    Butman, J.A.2    Brewer, C.3    Zalewski, C.4    Vortmeyer, A.O.5    Glenn, G.6    Oldfield, E.H.7    Lonser, R.R.8
  • 34
    • 77954572243 scopus 로고    scopus 로고
    • Genetic testing in Li-Fraumeni Syndrome: Uptake and psychosocial consequences
    • 20479422 10.1200/JCO.2009.27.2112
    • CRM Lammens NK Aaronson A Wagner, et al. 2010 Genetic testing in Li-Fraumeni Syndrome: uptake and psychosocial consequences J Clin Oncol 28 3008 3014 20479422 10.1200/JCO.2009.27.2112
    • (2010) J Clin Oncol , vol.28 , pp. 3008-3014
    • Lammens, C.R.M.1    Aaronson, N.K.2    Wagner, A.3
  • 35
    • 78650217249 scopus 로고    scopus 로고
    • Regular surveillance for Li-Fraumeni syndrome: Advice, adherence and perceived benefits
    • 20658357 1:STN:280:DC%2BC3cbms1OksA%3D%3D 10.1007/s10689-010-9368-z
    • CRM Lammens EMA Bleiker NK Aaronson, et al. 2010 Regular surveillance for Li-Fraumeni syndrome: advice, adherence and perceived benefits Fam Cancer 9 4 647 654 20658357 1:STN:280:DC%2BC3cbms1OksA%3D%3D 10.1007/s10689-010-9368-z
    • (2010) Fam Cancer , vol.9 , Issue.4 , pp. 647-654
    • Lammens, C.R.M.1    Bleiker, E.M.A.2    Aaronson, N.K.3
  • 36
    • 0020045180 scopus 로고
    • Prospective study of a family cancer syndrome
    • DOI 10.1001/jama.247.19.2692
    • FP Li JF Fraumeni 1982 Prospective study of a family cancer syndrome JAMA 247 2692 2694 7077763 1:STN:280:DyaL387pt1KhtA%3D%3D 10.1001/jama.247.19.2692 (Pubitemid 12105070)
    • (1982) Journal of the American Medical Association , vol.247 , Issue.19 , pp. 2692-2694
    • Li, F.P.1    Fraumeni Jr., J.F.2
  • 42
    • 67349284671 scopus 로고    scopus 로고
    • Radiological evaluation, management and surveillance of renal masses in von Hippel-Lindau disease
    • 19414081 1:STN:280:DC%2BD1MzitVymsA%3D%3D 10.1016/j.crad.2008.10.010
    • M Meister P Choyke C Anderson U Patel 2009 Radiological evaluation, management and surveillance of renal masses in Von Hippel-Lindau disease Clin Radiol 64 589 600 19414081 1:STN:280:DC%2BD1MzitVymsA%3D%3D 10.1016/j.crad.2008. 10.010
    • (2009) Clin Radiol , vol.64 , pp. 589-600
    • Meister, M.1    Choyke, P.2    Anderson, C.3    Patel, U.4
  • 43
    • 33744717863 scopus 로고    scopus 로고
    • Genotype phenotype correlation in Li-Fraumeni syndrome kindreds and its implications for management
    • DOI 10.1007/s10689-005-4522-8, Breast Cancer Treatment and Genetics
    • RN Moule SG Jhavar RA Eeles 2006 Genotype phenotype correlation in Li-Fraumeni syndrome kindreds and its implications for management Fam Cancer 5 129 133 16736281 1:STN:280:DC%2BD28zgslGrsw%3D%3D 10.1007/s10689-005-4522-8 (Pubitemid 43824468)
    • (2006) Familial Cancer , vol.5 , Issue.2 , pp. 129-133
    • Moule, R.N.1    Jhavar, S.G.2    Eeles, R.A.3
  • 44
    • 79954450460 scopus 로고    scopus 로고
    • NCCN © 2009 National Comprehensive Cancer Network, Inc. www.nccn.org. Accessed March 15, 2009. To view the most recent and complete version of the NCCN Guidelines, login to
    • NCCN (2008) The NCCN Clinical Practice Guidelines in Oncology™ Li-Fraumeni syndrome (Version 1.2008). © 2009 National Comprehensive Cancer Network, Inc. www.nccn.org. Accessed March 15, 2009. To view the most recent and complete version of the NCCN Guidelines, login to http://www.nccn.org
    • (2008) The NCCN Clinical Practice Guidelines in Oncology™ Li-Fraumeni Syndrome (Version 1.2008)
  • 46
    • 33646581703 scopus 로고    scopus 로고
    • Extrarenal rhabdoid tumors of soft tissue: Clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features
    • DOI 10.1111/j.1440-1827.2006.01962.x
    • Y Oda M Tsuneyoshi 2006 Extrarenal rhabdoid tumors of soft tissue: clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features Pathol Int 56 287 295 16704491 10.1111/j.1440-1827.2006.01962.x (Pubitemid 43725396)
    • (2006) Pathology International , vol.56 , Issue.6 , pp. 287-295
    • Oda, Y.1    Tsuneyoshi, M.2
  • 47
    • 0142157701 scopus 로고    scopus 로고
    • Li-fraumeni and related syndromes: Correlation between tumor type, family structure, and TP53 genotype
    • M Olivier DE Goldgar N Sodha, et al. 2003 Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype Cancer Res 63 6643 6650 14583457 1:CAS:528:DC%2BD3sXosVGgurs%3D (Pubitemid 37322942)
    • (2003) Cancer Research , vol.63 , Issue.20 , pp. 6643-6650
    • Olivier, M.1    Goldgar, D.E.2    Sodha, N.3    Ohgaki, H.4    Kleihues, P.5    Hainaut, P.6    Eeles, R.A.7
  • 49
    • 73049103985 scopus 로고    scopus 로고
    • Surveillance in von Hippel-Lindau disease (vHL)
    • 19863552 1:STN:280:DC%2BC3c%2FjvVWrug%3D%3D 10.1111/j.1399-0004.2009. 01281.x
    • MLM Poulsen E Budtz-Jørgensen ML Bisgaard 2010 Surveillance in von Hippel-Lindau disease (vHL) Clin Genet 77 49 59 19863552 1:STN:280: DC%2BC3c%2FjvVWrug%3D%3D 10.1111/j.1399-0004.2009.01281.x
    • (2010) Clin Genet , vol.77 , pp. 49-59
    • Poulsen, M.L.M.1    Budtz-Jørgensen, E.2    Bisgaard, M.L.3
  • 50
    • 0034126970 scopus 로고    scopus 로고
    • Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: A report from the National Wilms Tumor Study Group
    • MH Porteus P Narkool D Neuberg, et al. 2000 Characteristics and outcome of children with Beckwith-Wiedemann syndrome and Wilms' tumor: a report from the national Wilms tumor study group J Clin Oncol 18 2026 2031 10811666 1:STN:280:DC%2BD3c3ntF2qsg%3D%3D (Pubitemid 30324354)
    • (2000) Journal of Clinical Oncology , vol.18 , Issue.10 , pp. 2026-2031
    • Porteus, M.H.1    Narkool, P.2    Neuberg, D.3    Guthrie, K.4    Breslow, N.5    Green, D.M.6    Diller, L.7
  • 51
    • 33745471946 scopus 로고    scopus 로고
    • Benefits of screening in von Hippel-Lindau disease - Comparison of morbidity associated with initial tumours in affected parents and children
    • DOI 10.1159/000093008
    • M Priesemann KM Davies LA Perry, et al. 2006 Benefits of screening in von Hippel-Lindau disease-comparison of morbidity associated with initial tumours in affected parents and children Horm Res 66 1 5 16651847 1:CAS:528: DC%2BD28XmtVaktb8%3D 10.1159/000093008 (Pubitemid 43952580)
    • (2006) Hormone Research , vol.66 , Issue.1 , pp. 1-5
    • Priesemann, M.1    Davies, K.M.2    Perry, L.A.3    Drake, W.M.4    Chew, S.L.5    Monson, J.P.6    Savage, M.O.7    Johnston, L.B.8
  • 53
    • 38149091915 scopus 로고    scopus 로고
    • Genetic testing and tumor surveillance for children with cancer predisposition syndromes
    • 18197032 10.1097/MOP.0b013e3282f4249a
    • A Rao J Rothman KE Nichols 2008 Genetic testing and tumor surveillance for children with cancer predisposition syndromes Curr Opin Pediatr 20 1 7 18197032 10.1097/MOP.0b013e3282f4249a
    • (2008) Curr Opin Pediatr , vol.20 , pp. 1-7
    • Rao, A.1    Rothman, J.2    Nichols, K.E.3
  • 54
    • 64949113367 scopus 로고    scopus 로고
    • The SWI/SNF complex and cancer
    • 19234488 1:CAS:528:DC%2BD1MXktFOit70%3D 10.1038/onc.2009.4
    • D Reisman S Glaros EA Thompson 2009 The SWI/SNF complex and cancer Oncogene 28 1653 1668 19234488 1:CAS:528:DC%2BD1MXktFOit70%3D 10.1038/onc.2009.4
    • (2009) Oncogene , vol.28 , pp. 1653-1668
    • Reisman, D.1    Glaros, S.2    Thompson, E.A.3
  • 56
    • 0029934329 scopus 로고    scopus 로고
    • Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: Definition of an entity
    • LB Rorke RJ Packer JA Biegel 1996 Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: definition of an entity J Neurosurg 85 56 65 8683283 1:STN:280:DyaK283otF2gtg%3D%3D 10.3171/jns.1996.85.1. 0056 (Pubitemid 26195038)
    • (1996) Journal of Neurosurgery , vol.85 , Issue.1 , pp. 56-65
    • Rorke, L.B.1    Packer, R.J.2    Biegel, J.A.3
  • 57
    • 79954431664 scopus 로고    scopus 로고
    • Von Hippel-Lindau syndrome
    • Accessed15July2010
    • Schimke RN, Collins DL, Stolle CA (2009) von Hippel-Lindau syndrome. GeneReviews. http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part= vhl. Accessed 15 July 2010
    • (2009) GeneReviews
    • Schimke, R.N.1    Collins, D.L.2    Stolle, C.A.3
  • 59
    • 74549154987 scopus 로고    scopus 로고
    • Developmental defects and childhood cancer
    • 19812499 10.1097/MOP.0b013e328332c612
    • TP Slavin GL Wiesner 2009 Developmental defects and childhood cancer Curr Opin Pediatr 21 717 723 19812499 10.1097/MOP.0b013e328332c612
    • (2009) Curr Opin Pediatr , vol.21 , pp. 717-723
    • Slavin, T.P.1    Wiesner, G.L.2
  • 60
    • 33748870748 scopus 로고    scopus 로고
    • Hereditary cancer predisposition in children: Genetic basis and clinical implications
    • DOI 10.1002/ijc.21962
    • B Strahm D Malkin 2006 Hereditary cancer predisposition in children: genetic basis and clinical implications Int J Cancer 119 2001 2006 16642469 1:CAS:528:DC%2BD28XhtVSks7bK 10.1002/ijc.21962 (Pubitemid 44423655)
    • (2006) International Journal of Cancer , vol.119 , Issue.9 , pp. 2001-2006
    • Strahm, B.1    Malkin, D.2
  • 61
    • 58549117718 scopus 로고    scopus 로고
    • Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1
    • 19124645 1:CAS:528:DC%2BD1MXitFCqurs%3D 10.1136/jmg.2008.060152
    • JJ Swensen J Keyser CM Coffin, et al. 2009 Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1 J Med Genet 46 68 72 19124645 1:CAS:528:DC%2BD1MXitFCqurs%3D 10.1136/jmg.2008.060152
    • (2009) J Med Genet , vol.46 , pp. 68-72
    • Swensen, J.J.1    Keyser, J.2    Coffin, C.M.3
  • 62
    • 42049096998 scopus 로고    scopus 로고
    • Risk stratification in cancer predisposition syndromes: Lessons learned from novel molecular developments in Li-Fraumeni syndrome
    • DOI 10.1158/0008-5472.CAN-07-2091
    • U Tabori D Malkin 2008 Risk stratification in cancer predisposition syndromes: lessons learned from novel molecular developments in Li-Fraumeni syndrome Cancer Res 68 2053 2057 18381406 1:CAS:528:DC%2BD1cXktVyqtLY%3D 10.1158/0008-5472.CAN-07-2091 (Pubitemid 351521773)
    • (2008) Cancer Research , vol.68 , Issue.7 , pp. 2053-2057
    • Tabori, U.1    Malkin, D.2
  • 63
    • 33747437581 scopus 로고    scopus 로고
    • Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: A critical review of the evidence and suggested guidelines for local practice
    • DOI 10.1111/j.1440-1754.2006.00908.x
    • TY Tan DJ Amor 2006 Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practice J Paediatr Child Health 42 486 490 16925531 10.1111/j.1440-1754.2006.00908.x (Pubitemid 44252516)
    • (2006) Journal of Paediatrics and Child Health , vol.42 , Issue.9 , pp. 486-490
    • Tan, T.Y.1    Amor, D.J.2
  • 65
    • 0037222381 scopus 로고    scopus 로고
    • Germline TP53 mutations and Li-Fraumeni syndrome
    • DOI 10.1002/humu.10185
    • JM Varley 2003 Germline TP53 mutations and Li-Fraumeni syndrome Hum Mutat 21 313 320 12619118 1:CAS:528:DC%2BD3sXis1yjtLc%3D 10.1002/humu.10185 (Pubitemid 36292974)
    • (2003) Human Mutation , vol.21 , Issue.3 , pp. 313-320
    • Varley, J.M.1
  • 66
    • 65349103899 scopus 로고    scopus 로고
    • Blinded by the light: The growing complexity of p53
    • 19410540 1:CAS:528:DC%2BD1MXlvFams74%3D 10.1016/j.cell.2009.04.037
    • KH Vousden C Prives 2009 Blinded by the light: The growing complexity of p53 Cell 137 413 431 19410540 1:CAS:528:DC%2BD1MXlvFams74%3D 10.1016/j.cell.2009.04.037
    • (2009) Cell , vol.137 , pp. 413-431
    • Vousden, K.H.1    Prives, C.2
  • 69
    • 77149130213 scopus 로고    scopus 로고
    • Beckwith-Wiedemann syndrome
    • 19550435 10.1038/ejhg.2009.106
    • R Weksberg C Shuman JB Beckwith 2010 Beckwith-Wiedemann syndrome Eur J Hum Genet 18 8 14 19550435 10.1038/ejhg.2009.106
    • (2010) Eur J Hum Genet , vol.18 , pp. 8-14
    • Weksberg, R.1    Shuman, C.2    Beckwith, J.B.3
  • 70
    • 68049114587 scopus 로고    scopus 로고
    • Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol
    • 19610116 1:CAS:528:DC%2BD1MXhtVekurzJ 10.1002/ajmg.a.32966
    • YA Zarate R Mena LJ Martin, et al. 2009 Experience with hemihyperplasia and Beckwith-Wiedemann syndrome surveillance protocol Am J Med Genet 149A 1691 1697 19610116 1:CAS:528:DC%2BD1MXhtVekurzJ 10.1002/ajmg.a.32966
    • (2009) Am J Med Genet , vol.149 , pp. 1691-1697
    • Zarate, Y.A.1    Mena, R.2    Martin, L.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.