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Volumn 14, Issue 6, 2008, Pages 1445-1451

Carrier detection of phenylketonuria in Iranian families by variable number tandem-repeat polymorphism analysis

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

EID: 59949098145     PISSN: 10203397     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (17)
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    • Følling A. Ueber Ausscheidung von Phenylbrenztraubensaeure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillitaet [The excretion of phenylpyruvic acid in the urine, an anomaly of metabolism in connection with imbecility]. Zeitschrift für physiologische Chemie, 1934, 227:169-76.
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  • 3
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    • Hyperphenylalaninemia: Phenylalanine hydroxylase deficiency
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    • (2001) The metabolic and molecular bases of inherited disease , pp. 1667-1724
    • Scriver, C.R.1    Kaufman, S.2
  • 4
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    • Inherited metabolic disorders in Turkey
    • Ozalp I et al. Inherited metabolic disorders in Turkey. Journal of inherited metabolic disease, 1990, 13(5):732-8.
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    • 0028287655 scopus 로고
    • Phenylketonuria in Turkey, Ireland, and West Scotland
    • Woolf LI. Phenylketonuria in Turkey, Ireland, and West Scotland. Journal of inherited metabolic disease, 1994, 17(2):246-7.
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    • Woolf, L.I.1
  • 7
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    • Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria
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    • (1983) Nature , vol.306 , Issue.5939 , pp. 151-155
    • Woo, S.L.1
  • 8
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  • 10
    • 0028673284 scopus 로고
    • A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria
    • Eisensmith CR, Goltsov AA, Woo SLC. A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria. Prenatal diagnosis, 1994, 14(12):1113-8.
    • (1994) Prenatal diagnosis , vol.14 , Issue.12 , pp. 1113-1118
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  • 11
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.