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Volumn 34, Issue 3, 1997, Pages 250-251

Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal

Author keywords

Amniotic fluid; FMRP; Fragile X syndrome; Prenatal diagnosis

Indexed keywords

ANTIBODY;

EID: 0031020588     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.34.3.250     Document Type: Article
Times cited : (22)

References (10)
  • 1
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    • (1995) Lancet , vol.345 , pp. 1147-1148
    • Willemsen, R.1    Mohkamsing, S.2    De Vries, B.3
  • 2
    • 16944366572 scopus 로고    scopus 로고
    • Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique
    • in press
    • Willemsen R, Smits A, Mohkamsing S, et al. Rapid antibody test for diagnosing fragile X syndrome: a validation of the technique. Hum Genet (in press).
    • Hum Genet
    • Willemsen, R.1    Smits, A.2    Mohkamsing, S.3
  • 3
    • 0025833298 scopus 로고
    • Absence of expression of the FMR-1 gene in fragile X syndrome
    • Pieretti M, Zhang FP, Fu YH, et al. Absence of expression of the FMR-1 gene in fragile X syndrome. Cell 1991;66:817-22.
    • (1991) Cell , vol.66 , pp. 817-822
    • Pieretti, M.1    Zhang, F.P.2    Fu, Y.H.3
  • 4
    • 0026951222 scopus 로고
    • Methylation analysis of CGG sites in the CpG island of the human FMR1 gene
    • Hansen RS, Gartler SM, Scott CR, et al. Methylation analysis of CGG sites in the CpG island of the human FMR1 gene. Hum Mol Genet 1992;1:571-8.
    • (1992) Hum Mol Genet , vol.1 , pp. 571-578
    • Hansen, R.S.1    Gartler, S.M.2    Scott, C.R.3
  • 6
    • 0027236971 scopus 로고
    • Characterization and localization of the FMR-1 gene product associated with fragile X syndrome
    • Verheij C, Bakker CE, de Graaff E, et al. Characterization and localization of the FMR-1 gene product associated with fragile X syndrome. Nature 1993;363:722-4.
    • (1993) Nature , vol.363 , pp. 722-724
    • Verheij, C.1    Bakker, C.E.2    De Graaff, E.3
  • 7
    • 0025952727 scopus 로고
    • Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation
    • Rousseau F, Heitz D, Biancalana V, et al. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation. N Engl J Med 1991;325:1673-81.
    • (1991) N Engl J Med , vol.325 , pp. 1673-1681
    • Rousseau, F.1    Heitz, D.2    Biancalana, V.3
  • 9
    • 0026777136 scopus 로고
    • Intragenic probe used for diagnostics in fragile X families
    • Verkerk AJ, de Vries BB, Niermeijer MF, et al. Intragenic probe used for diagnostics in fragile X families. Am J Med Genet 1992;43:192-6.
    • (1992) Am J Med Genet , vol.43 , pp. 192-196
    • Verkerk, A.J.1    De Vries, B.B.2    Niermeijer, M.F.3
  • 10
    • 85046113287 scopus 로고    scopus 로고
    • A new approach for prenatal diagnosis of fragile X syndrome
    • Willemsen R, Oosterwijk JC, Los FJ, et al. A new approach for prenatal diagnosis of fragile X syndrome. Lancet 1996; 348:967-8.
    • (1996) Lancet , vol.348 , pp. 967-968
    • Willemsen, R.1    Oosterwijk, J.C.2    Los, F.J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.