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Volumn 64, Issue 4, 2000, Pages 329-339

Genetic diversity at the FMR1 locus in the Indonesian population

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; DNA POLYMORPHISM; GENE FREQUENCY; GENE LOCUS; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; HUMAN CELL; HUMAN EXPERIMENT; INDONESIA; MALE; NORMAL HUMAN; PRIORITY JOURNAL; TANDEM REPEAT;

EID: 0033786969     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1017/S0003480000008204     Document Type: Article
Times cited : (21)

References (20)
  • 1
    • 0027500851 scopus 로고
    • Data on the CGG repeat on the fragile X site in the non-retarded Japanese population and family suggest the presence of a subgroup of normal alleles predisposing to mutate
    • (1993) Hum. Genet , vol.92 , pp. 431-436
    • Arinami, T.1    Asano, M.2    Kobayashi, K.3
  • 8
    • 0026345716 scopus 로고
    • Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
    • (1991) Cell , vol.67 , pp. 1047-1058
    • Fu, J.H.1    Kuhl, D.P.2    Pizzuti, A.3
  • 15
    • 0026316183 scopus 로고
    • Fragile X syndrome: Genetic localisation by genetic mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site
    • (1991) J. Med. Genet , vol.28 , pp. 818-823
    • Richards, R.I.1    Holman, K.2    Kozman, H.3
  • 18
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in the fragile X syndrome
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, J.S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.