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Volumn 11, Issue 1, 1997, Pages 81-83

Detection of microsatellites by ethidium bromide staining. The analysis of an STR system in the human phenylalanine hydroxylase gene

Author keywords

Microsatellite; Phenylketonuria; STR

Indexed keywords

ETHIDIUM BROMIDE; MICROSATELLITE DNA; PHENYLALANINE 4 MONOOXYGENASE;

EID: 0031079613     PISSN: 08908508     EISSN: None     Source Type: Journal    
DOI: 10.1006/mcpr.1996.0082     Document Type: Article
Times cited : (7)

References (12)
  • 3
    • 0028888322 scopus 로고
    • Molecular genetics of phenylketonuria: From molecular antro- pology to gene therapy
    • Eisensmith R. C., Woo S. L. C. Molecular genetics of phenylketonuria: from molecular antro- pology to gene therapy. Advances in Genetics. 32:1995;199-271.
    • (1995) Advances in Genetics , vol.32 , pp. 199-271
    • Eisensmith, R.C.1    Woo, S.L.C.2
  • 7
    • 0027287605 scopus 로고
    • A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria
    • Goltsov A. A., Eisensmith R. C., Naughton E. R., Jin L., Chakraborty R., Woo S. L. C. A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria. Human Molecular Genetics. 5:1993;577-581.
    • (1993) Human Molecular Genetics , vol.5 , pp. 577-581
    • Goltsov, A.A.1    Eisensmith, R.C.2    Naughton, E.R.3    Jin, L.4    Chakraborty, R.5    Woo, S.L.C.6
  • 9
    • 0028673284 scopus 로고
    • A simple, rapid and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria
    • Eisensmith R. C., Goltsov A. A., Woo S. L. C. A simple, rapid and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria. Prenatal Diagnosis. 14:1994;1113-1118.
    • (1994) Prenatal Diagnosis , vol.14 , pp. 1113-1118
    • Eisensmith, R.C.1    Goltsov, A.A.2    Woo, S.L.C.3
  • 10
    • 0027287605 scopus 로고
    • A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria
    • Goltsov A. A., Eisensmith R. C., Naughton E. R., Jin L., Chakraborty R., Woo S. L. C. A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria. Human Molecular Genetics. 2:1993;577-581.
    • (1993) Human Molecular Genetics , vol.2 , pp. 577-581
    • Goltsov, A.A.1    Eisensmith, R.C.2    Naughton, E.R.3    Jin, L.4    Chakraborty, R.5    Woo, S.L.C.6
  • 11
    • 0028117652 scopus 로고
    • Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria
    • Romano V., Dianzani I., Ponzone A. Prenatal diagnosis by minisatellite analysis in Italian families with phenylketonuria. Prenatal Diagnosis. 14:1994;959-962.
    • (1994) Prenatal Diagnosis , vol.14 , pp. 959-962
    • Romano, V.1    Dianzani, I.2    Ponzone, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.