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Volumn 101, Issue 2, 1997, Pages 214-218

Sequence analysis of long FMR1 arrays in the Japanese population:Insights into the generation of long [CGG)(n) tracts

Author keywords

[No Author keywords available]

Indexed keywords

REPETITIVE DNA;

EID: 0031457067     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050618     Document Type: Article
Times cited : (14)

References (23)
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    • Arinami T, Asano M, Kobayashi K, Yanagi H, Hamaguchi H (1993) Data on the CGG repeat at the fragile-X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate. Hum Genet 92: 431-436
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  • 2
    • 0028184174 scopus 로고
    • High resolution of human evolutionary trees with polymorphic microsatellites
    • Bowcock A, Ruiz-Linares A, Minch E, Kidd K, Cavalli-Sforza L (1994) High resolution of human evolutionary trees with polymorphic microsatellites. Nature 368: 455-457
    • (1994) Nature , vol.368 , pp. 455-457
    • Bowcock, A.1    Ruiz-Linares, A.2    Minch, E.3    Kidd, K.4    Cavalli-Sforza, L.5
  • 4
    • 0028886722 scopus 로고
    • Population survey of the human FRM1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions
    • Eichler E, Hammond H, MacPherson J, Ward P, Nelson D (1995) Population survey of the human FRM1 CGG repeat substructure suggests biased polarity for the loss of AGG interruptions. Hum Mol Genet 4: 2199-2208
    • (1995) Hum Mol Genet , vol.4 , pp. 2199-2208
    • Eichler, E.1    Hammond, H.2    MacPherson, J.3    Ward, P.4    Nelson, D.5
  • 5
    • 0029916569 scopus 로고    scopus 로고
    • Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile-X syndrome
    • Eichler E, MacPherson J, Murray A, Jacobs P, Chakravarti A, Nelson D (1996) Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile-X syndrome. Hum Mol Genet 5: 319-330
    • (1996) Hum Mol Genet , vol.5 , pp. 319-330
    • Eichler, E.1    MacPherson, J.2    Murray, A.3    Jacobs, P.4    Chakravarti, A.5    Nelson, D.6
  • 7
    • 0029156798 scopus 로고
    • FMR1 triplet arrays: Paying the price of perfection
    • Hirst M (1995) FMR1 triplet arrays: paying the price of perfection. J Med Genet 32: 761-763
    • (1995) J Med Genet , vol.32 , pp. 761-763
    • Hirst, M.1
  • 9
    • 0028133504 scopus 로고
    • Precursor arrays for triplet repeat expansion at the fragile-X locus
    • Hirst M, Grewal P, Davies K (1994) Precursor arrays for triplet repeat expansion at the fragile-X locus. Hum Mol Genet 3: 1553-1560
    • (1994) Hum Mol Genet , vol.3 , pp. 1553-1560
    • Hirst, M.1    Grewal, P.2    Davies, K.3
  • 10
    • 0028894410 scopus 로고
    • Recent African origin of modem humans revealed by complete sequence analysis of mitochondrial DNAs
    • Horai S, Hayasaka K, Kondo R, Tsugane K, Takahata N (1995) Recent African origin of modem humans revealed by complete sequence analysis of mitochondrial DNAs. Proc Natl Acad Sci USA 92: 532-536
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 532-536
    • Horai, S.1    Hayasaka, K.2    Kondo, R.3    Tsugane, K.4    Takahata, N.5
  • 12
    • 0028360849 scopus 로고
    • Cryptic and polar variation of the fragile-X repeat could result in predisposing normal alleles
    • Kunst C, Warren S (1994) Cryptic and polar variation of the fragile-X repeat could result in predisposing normal alleles. Cell 77: 853-861
    • (1994) Cell , vol.77 , pp. 853-861
    • Kunst, C.1    Warren, S.2
  • 15
    • 0027416537 scopus 로고
    • Linkage disequilibrium between the fragile-X mutation and two closely linked CA repeats suggests that fragile-X chromosomes are derived from a small number of founder chromosomes
    • Oudet C, Mornet E, Serre J, Thomas F, Lentes-Zengerling S, Kretz C, Deluchat C, Tejada I, Boue A, Mandel J (1993) Linkage disequilibrium between the fragile-X mutation and two closely linked CA repeats suggests that fragile-X chromosomes are derived from a small number of founder chromosomes. Am J Hum Genet 52: 297-304
    • (1993) Am J Hum Genet , vol.52 , pp. 297-304
    • Oudet, C.1    Mornet, E.2    Serre, J.3    Thomas, F.4    Lentes-Zengerling, S.5    Kretz, C.6    Deluchat, C.7    Tejada, I.8    Boue, A.9    Mandel, J.10
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    • Sequence analysis of the fragile-X trinucleotide repeat: Implications for the origin of the fragile-X mutation
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    • Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population
    • Zhong N, Liu X, Gou S, Houck G, Li S, Dobkin C, Brown W (1994) Distribution of FMR-1 and associated microsatellite alleles in a normal Chinese population. Am J Med Genet 51: 417-422
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    • Zhong, N.1    Liu, X.2    Gou, S.3    Houck, G.4    Li, S.5    Dobkin, C.6    Brown, W.7
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.