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Volumn 1, Issue 3, 1996, Pages 227-231

Point mutation analysis of the FMR-1 gene in autism

Author keywords

ASO analysis; Association; Autism; FMR 1; Genetic; Intronic; Polymorphism; Sequencing; SSCP

Indexed keywords

FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN; NERVE PROTEIN; RNA BINDING PROTEIN;

EID: 0030180314     PISSN: 13594184     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (22)

References (21)
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  • 13
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    • Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing
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    • Autosomal recessive ocular albinism associated with a functionally significant tyrosine hydroxylase gene polymorphism
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    • (1995) Nature Genet , vol.9 , pp. 92-95
    • Fukai, K.1    Holmes, S.A.2    Lucchese, N.J.3    Mok Siu, V.4    Weleber, R.G.5    Schnur, R.E.6    Spritz, R.A.7
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    • Splice junctions, branch point sites, and exons: Sequence statistics, identification, and applications to the genome project
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    • Coulondre, C.1    Miller, J.H.2    Farabangh, P.J.3    Gilbert, W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.