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BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

101 related articles for article (PubMed ID: 4666577)

  • 21. [Galactosemia as based on the records of Department I of Pediatrics of the Silesian Medical Academy].
    Hager-Malecka B; Sychlowy A; Szczepański Z
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    Ionăşescu V; Luca N
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    Klethi J
    C R Seances Soc Biol Fil; 1973; 167(10):1461-6. PubMed ID: 4793567
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    Kelly S; Desjardins L; Khera SA
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    Helv Paediatr Acta; 1967 Jul; 22(3):252-7. PubMed ID: 5590140
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    Wiśniewski L; Wrede A
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    [No Abstract]   [Full Text] [Related]  

  • 28. [Acute galactosemia].
    Hosková A
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    [No Abstract]   [Full Text] [Related]  

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