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Volumn 4, Issue 12, 2003, Pages 769-771

Identification and high-resolution mapping of constitutional 11q deletion in an infant with multifocal neuroblastoma

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT;

EID: 0347503601     PISSN: 14702045     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1470-2045(03)01283-X     Document Type: Article
Times cited : (31)

References (11)
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    • (2002) Principles and Practice of Pediatric Oncology , pp. 895-938
    • Brodeur, G.M.1    Maris, J.M.2
  • 2
    • 0033034390 scopus 로고    scopus 로고
    • Molecular biology of neuroblastoma
    • Maris JM, Matthay KK. Molecular biology of neuroblastoma. J Clin Oncol 1999; 17: 2264-79.
    • (1999) J. Clin. Oncol. , vol.17 , pp. 2264-2279
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  • 3
    • 0035166044 scopus 로고    scopus 로고
    • Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma
    • Maris JM, Guo C, White PS, et al. Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma. Med Pediatr Oncol 2001; 36: 24-27.
    • (2001) Med. Pediatr. Oncol. , vol.36 , pp. 24-27
    • Maris, J.M.1    Guo, C.2    White, P.S.3
  • 4
    • 0033517349 scopus 로고    scopus 로고
    • Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas
    • Guo C, White PS, Weiss MJ, et al. Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas. Oncogene 1999; 18: 4948-57.
    • (1999) Oncogene , vol.18 , pp. 4948-4957
    • Guo, C.1    White, P.S.2    Weiss, M.J.3
  • 5
    • 0025315791 scopus 로고
    • Constitutional deletions predisposing to retinoblastoma
    • Janson M, Kock E, Nordenskjold M. Constitutional deletions predisposing to retinoblastoma. Hum Genet 1990; 85: 21-24.
    • (1990) Hum. Genet. , vol.85 , pp. 21-24
    • Janson, M.1    Kock, E.2    Nordenskjold, M.3
  • 6
    • 0025828557 scopus 로고
    • Evidence for WT1 as a Wilms' tumour (WT) gene: Intragenic germinal deletion in bilateral WT
    • Huff V, Miwa H, Haber DA, et al. Evidence for WT1 as a Wilms' tumour (WT) gene: intragenic germinal deletion in bilateral WT. Am J Hum Genet 1991; 48: 997-1003.
    • (1991) Am. J. Hum. Genet. , vol.48 , pp. 997-1003
    • Huff, V.1    Miwa, H.2    Haber, D.A.3
  • 7
    • 0027476712 scopus 로고
    • Constitutional 1p36 deletion in a child with neuroblastoma
    • Biegel JA, White PS, Marshall HN, et al. Constitutional 1p36 deletion in a child with neuroblastoma. Am J Hum Genet 1993; 52: 176-82.
    • (1993) Am. J. Hum. Genet. , vol.52 , pp. 176-182
    • Biegel, J.A.1    White, P.S.2    Marshall, H.N.3
  • 8
    • 0029164456 scopus 로고
    • Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q
    • Koiffmann CP, Gonzalez CH, Vianna-Morgante AM, et al. Neuroblastoma in a boy with MCA/MR syndrome, deletion 11q, and duplication 12q. Am J Med Genet 1995; 58: 46-49.
    • (1995) Am. J. Med. Genet. , vol.58 , pp. 46-49
    • Koiffmann, C.P.1    Gonzalez, C.H.2    Vianna-Morgante, A.M.3
  • 9
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    • Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q
    • Tunnacliffe A, Jones C, Le Paslier D, et al. Localization of Jacobsen syndrome breakpoints on a 40-Mb physical map of distal chromosome 11q. Genome Res 1999; 9: 44-52.
    • (1999) Genome Res. , vol.9 , pp. 44-52
    • Tunnacliffe, A.1    Jones, C.2    Le Paslier, D.3
  • 10
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    • Clinical and molecular characterization of patients with distal 11q deletions
    • Penny LA, Dell'Aquila M, Jones MC, et al. Clinical and molecular characterization of patients with distal 11q deletions. Am J Hum Genet 1995; 56: 676-83.
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    • Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13
    • Maris JM, Weiss MJ, Mosse Y, et al. Evidence for a hereditary neuroblastoma predisposition locus at chromosome 16p12-13. Cancer Res 2002; 62: 6651-58.
    • (2002) Cancer Res. , vol.62 , pp. 6651-6658
    • Maris, J.M.1    Weiss, M.J.2    Mosse, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.