메뉴 건너뛰기




Volumn 23, Issue 2, 1994, Pages 486-489

Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3

Author keywords

[No Author keywords available]

Indexed keywords


EID: 0027968936     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1994.1528     Document Type: Article
Times cited : (37)

References (19)
  • 2
    • 0027231001 scopus 로고
    • Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study
    • Evans, D. G. R., Ladusans, E. J., Rimmer, S., Burnell, L D, Thakkar, N., and Famdon, P. A. (1993). Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study. J. Med. Genet. 30: 460-464.
    • (1993) J. Med. Genet. , vol.30 , pp. 460-464
    • Evans, D.G.R.1    Ladusans, E.J.2    Rimmer, S.3    Burnell, L.D.4    Thakkar, N.5    Famdon, P.A.6
  • 4
    • 33645411169 scopus 로고
    • Evidence for a tumor suppressor gene on chromosome 9 in basal cell carcinomas of the skin
    • Gailani, M. R., Keffell, D. J., and Bale, A. E. (1991). Evidence for a tumor suppressor gene on chromosome 9 in basal cell carcinomas of the skin. Am. J. Hum. Genet. 49(Suppl.): A454.
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. A454
    • Gailani, M.R.1    Keffell, D.J.2    Bale, A.E.3
  • 6
    • 0023222358 scopus 로고
    • Nevoid basal cell carcinoma syndrome
    • Gorlin, R. J. (1987). Nevoid basal cell carcinoma syndrome. Medicine 66: 98-113.
    • (1987) Medicine , vol.66 , pp. 98-113
    • Gorlin, R.J.1
  • 11
    • 0024314891 scopus 로고
    • MAP, an expert system for multiple pairwise linkage analysis
    • Morton, N. E., and Andrews, V. (1989). MAP, an expert system for multiple pairwise linkage analysis. Ann. Hum. Genet. 53: 263-269.
    • (1989) Ann. Hum. Genet. , vol.53 , pp. 263-269
    • Morton, N.E.1    Andrews, V.2
  • 12
    • 0017192186 scopus 로고
    • A computer program for linkage analysis of general human pedigrees
    • Ott, J. (1976). A computer program for linkage analysis of general human pedigrees. Am. J. Hum. Genet. 28: 528-529.
    • (1976) Am. J. Hum. Genet. , vol.28 , pp. 528-529
    • Ott, J.1
  • 13
    • 0018075145 scopus 로고
    • A simple scheme for the analysis of HLA linkages in pedigrees
    • Ott, J. (1978). A simple scheme for the analysis of HLA linkages in pedigrees. Ann. Hum. Genet. 42: 255-257.
    • (1978) Ann. Hum. Genet. , vol.42 , pp. 255-257
    • Ott, J.1
  • 14
    • 0003408936 scopus 로고
    • Johns Hopkins Univ. Press, Baltimore, MD
    • Ott, J. (1991). ''Analysis of Human Genetic Linkage," 2nd ed., pp. 136-141, Johns Hopkins Univ. Press, Baltimore, MD.
    • (1991) Analysis of Human Genetic Linkage , pp. 136-141
    • Ott, J.1
  • 17
    • 0026878842 scopus 로고
    • Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9
    • Strathdee, C. A., Duncan, A. M. V., and Buchwald, M. (1992). Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9. Nature Genet. 1: 196-198.
    • (1992) Nature Genet , vol.1 , pp. 196-198
    • Strathdee, C.A.1    Duncan, A.M.V.2    Buchwald, M.3
  • 19
    • 0019974447 scopus 로고
    • Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anaemia and xeroderma pigmentosum families
    • Welshimer, K., and Swift, M. (1982). Congenital malformations and developmental disabilities in ataxia-telangiectasia, Fanconi anaemia and xeroderma pigmentosum families. Am. J. Hum. Genet. 34: 781-793.
    • (1982) Am. J. Hum. Genet. , vol.34 , pp. 781-793
    • Welshimer, K.1    Swift, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.