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Volumn 38, Issue 3, 2002, Pages 193-199

Neuroblastoma in a patient with the Beckwith-Wiedemann syndrome (BWS)

Author keywords

Beckwith Wiedeman syndrome; Childhood cancer; Neuroblastoma; Screening

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CANCER SCREENING; CASE REPORT; CHILD; CHILDHOOD CANCER; CHROMOSOME 11P; CLINICAL EXAMINATION; COMPUTER ASSISTED TOMOGRAPHY; CONFERENCE PAPER; DISEASE ASSOCIATION; FEMALE; HETEROZYGOSITY LOSS; HUMAN; NEUROBLASTOMA; PRIORITY JOURNAL;

EID: 0036182470     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/mpo.1310     Document Type: Article
Times cited : (9)

References (33)
  • 10
    • 0031915657 scopus 로고    scopus 로고
    • Children at increased risk for Wilms tumor: Monitoring issues
    • (1998) J Pediatr , vol.132 , pp. 377-379
    • Beckwith, J.B.1
  • 14
    • 0031940675 scopus 로고    scopus 로고
    • Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann Syndrome Registry
    • (1998) J Pediatr , vol.132 , pp. 398-400
    • DeBaun, M.R.1    Tucker, M.A.2
  • 18
    • 0033609117 scopus 로고    scopus 로고
    • Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 5203-5208
    • Lee, M.P.1    DeBaun, M.R.2    Mitsuya, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.