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Volumn 50, Issue 3, 2001, Pages 337-344

A novel WT1 gene mutation associated with Wilms' tumor and congenital male genitourinary malformation

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 11; CONTROLLED STUDY; EXON; GENE; GENE MUTATION; GENE WT1; HETEROZYGOSITY; HUMAN; HUMAN CELL; INTRON; KIDNEY DISEASE; MALE GENITAL SYSTEM; NEPHROBLASTOMA; POINT MUTATION; PRIORITY JOURNAL; TUMOR CELL; UROGENITAL TRACT MALFORMATION;

EID: 0034874335     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-200109000-00008     Document Type: Article
Times cited : (13)

References (51)
  • 14
    • 0017236069 scopus 로고
    • Congenital anomalies in children with Wilms' tumor: A new survey
    • (1976) Cancer , vol.37 , pp. 403-408
    • Pendergrass, T.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.