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Volumn 53, Issue 4, 1998, Pages 278-280

Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome

Author keywords

Cytogenetics; Del(2)(q37) syndrome; Tumor susceptibility gene; Wilms' tumor

Indexed keywords

ARTICLE; CANCER SUSCEPTIBILITY; CASE REPORT; CHROMOSOME 2; CHROMOSOME DELETION; FEMALE; GENE MAPPING; GONADAL DYSGENESIS; HUMAN; NEPHROBLASTOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; UTERUS BICORNIS;

EID: 0031981781     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1998.tb02696.x     Document Type: Article
Times cited : (27)

References (7)
  • 1
    • 0028813978 scopus 로고
    • Brachydactyly and mental retardation: An Albright Hereditary Osteodystrophy-like syndrome localized to 2q37
    • Wilson LC, Leverton K, Oude Luttikhuis MEM, et al. Brachydactyly and mental retardation: an Albright Hereditary Osteodystrophy-like syndrome localized to 2q37. Am J Hum Genet 1995: 56: 400-407.
    • (1995) Am J Hum Genet , vol.56 , pp. 400-407
    • Wilson, L.C.1    Leverton, K.2    Oude Luttikhuis, M.E.M.3
  • 2
    • 0029038024 scopus 로고
    • Clinical phenotype associated with terminal 2q37 deletion
    • Conrad B, Dewald G, Christensen E, et al. Clinical phenotype associated with terminal 2q37 deletion. Clin Genet 1995: 48: 134-139.
    • (1995) Clin Genet , vol.48 , pp. 134-139
    • Conrad, B.1    Dewald, G.2    Christensen, E.3
  • 3
    • 0029080844 scopus 로고
    • Albright hereditary osteodystrophy and del (2)(q37.3) in four unrelated individuals
    • Phelan MC, Rogers RC, Clarkson KB, et al. Albright hereditary osteodystrophy and del (2)(q37.3) in four unrelated individuals. Am. J. Med Genet 1995: 58: 1-7.
    • (1995) Am. J. Med Genet , vol.58 , pp. 1-7
    • Phelan, M.C.1    Rogers, R.C.2    Clarkson, K.B.3
  • 6
    • 0030965752 scopus 로고    scopus 로고
    • Common and variant gene fusions predict distinct clinical phenotypes in rhabdomyosarcoma
    • Kelly KM, Womer RB, Sorensen PH, Xiong QB, Bart FG. Common and variant gene fusions predict distinct clinical phenotypes in rhabdomyosarcoma. J Clin Oncol 1997: 15: 1831-1836.
    • (1997) J Clin Oncol , vol.15 , pp. 1831-1836
    • Kelly, K.M.1    Womer, R.B.2    Sorensen, P.H.3    Xiong, Q.B.4    Bart, F.G.5
  • 7
    • 0025788974 scopus 로고
    • WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
    • Pelletier J, Bruening W, Li FP, et al. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature 1991: 353: 431-434.
    • (1991) Nature , vol.353 , pp. 431-434
    • Pelletier, J.1    Bruening, W.2    Li, F.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.