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Volumn 125 A, Issue 3, 2004, Pages 320-

Fragile X Carrier Screening and Spinocerebellar Ataxia in Older Males [3]

Author keywords

[No Author keywords available]

Indexed keywords

AGE; CLINICAL FEATURE; DIFFUSION WEIGHTED IMAGING; FRAGILE X SYNDROME; GENE LOCUS; GENETIC SCREENING; HETEROZYGOTE DETECTION; HUMAN; LETTER; MALE; MENTAL DEFICIENCY; MOLECULAR GENETICS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SPINOCEREBELLAR DEGENERATION; WHITE MATTER;

EID: 1542378696     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (30)

References (5)
  • 2
    • 0037084852 scopus 로고    scopus 로고
    • Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles
    • Dombrowski C, Levesque S, Morel ML, Rouillard P, Morgan K, Rousseau F. 2002. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. Hum Mol Genet 11:371-378.
    • (2002) Hum Mol Genet , vol.11 , pp. 371-378
    • Dombrowski, C.1    Levesque, S.2    Morel, M.L.3    Rouillard, P.4    Morgan, K.5    Rousseau, F.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.