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Volumn 68, Issue 2, 2001, Pages 355-363

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; ECHOGRAPHY; FEMALE; GENE SEGREGATION; GENEALOGY; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HETEROZYGOTE; HUMAN; KIDNEY POLYCYSTIC DISEASE; LIVER POLYCYSTIC DISEASE; MALE; PEDIGREE; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0035125616     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318188     Document Type: Article
Times cited : (136)

References (44)
  • 3
    • 0031035050 scopus 로고    scopus 로고
    • Loss of the polycystic kidney disease (PKD1) region of chromosome 16p13.3 in renal cysts supports a loss-of-function model for cyst pathogenesis
    • (1997) J Clin Invest , vol.99 , pp. 194-199
    • Brasier, J.1    Henske, E.2
  • 11
    • 0032869122 scopus 로고    scopus 로고
    • Autosomal dominant polycystic kidney disease: Clues to pathogenesis
    • (1999) Hum Mol Genet , vol.8 , pp. 1861-1869
    • Harris, P.C.1
  • 33
    • 0029945706 scopus 로고    scopus 로고
    • Descent graphs in pedigree analysis: Applications to haplotyping location scores, and marker-sharing statistics
    • (1996) Am J Hum Genet , vol.58 , pp. 1323-1337
    • Sobel, E.1    Lange, K.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.