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Records found: 11  
Your query: Author Sysno/Doc.kind = "^sllk_un_auth p0056048 xaec^"

  1. 1.A double germline mutations in the APC and p53 genes

    A double germline mutations in the APC and p53 genes  / V. Zajac ... [et al.] .  Neoplasma : journal of experimental and clinical oncology. - ISSN 0028-2685 . - Roč. 47, č. 6 (2000), s. 335-341  : Graf  
    C 720
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  2. 2.Age and Geographical Distribution in Families with BRCA1/BRCA2 Mutations in the Slovak Republic

    Age and Geographical Distribution in Families with BRCA1/BRCA2 Mutations in the Slovak Republic  / Ciernikova S. ... [et al.] .  Hereditary cancer in clinical practice . - 2006; 4(1): 7–11   [Dokument nie je vo fonde knižnice]
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  3. 3.Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families

    Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families  / S. Čierniková ... [et al.] .  Neoplasma : journal of experimental and clinical oncology. - ISSN 0028-2685 . - Vol. 53, no. 2 (2006), s. 97-102  : obr., tab.  
    C 720
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  4. 4.Characterization of APC exon 15 germ-line mutation in FAP family with severe phenotype showing extracolonic symptoms

    Characterization of APC exon 15 germ-line mutation in FAP family with severe phenotype showing extracolonic symptoms  / T. Kirchhoff ... [et al.] .  Neoplasma : journal of experimental and clinical oncology. - ISSN 0028-2685 . - Roč. 46, č. 5 (1999), s. 290-294  : Graf, obr.  
    C 720
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  5. 5.Molekulová analýza prognosticky významných markerov chronickej lymfocytovej leukémie

    Molekulová analýza prognosticky významných markerov chronickej lymfocytovej leukémie  / Erika Tomková ... [et al.] .  Newslab : časopis laboratórnej medicíny. - ISSN 1338-9661 . - Roč. 8, č. 1 (2017), s. 38-43  : ilustr. fareb. grafy, obr.  
    C 3151
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  6. 6.Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene

    Multiple gynecologic tumors as rare associated phenotypes of FAP/Gardner syndrome in a family with the novel germline mutation in the APC gene  / M. Kováč ... [et al.] .  Clinical genetics . - Vol. 69, no. 2 (2006), s. 183-186   [Dokument nie je vo fonde knižnice]
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  7. 7.Mutation screening of the BRCA1 gene in Slovak patients

    Mutation screening of the BRCA1 gene in Slovak patients  / M. Tomka ... [et al.] .  Neoplasma : journal of experimental and clinical oncology. - ISSN 0028-2685 . - Roč. 48, č. 6 (2001), s. 451-455  : Graf, obr.  
    C 720
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  8. 8.Odysea čítania DNA

    Odysea čítania DNA  / Radka Tomášová ... [et al.] .  Newslab : časopis laboratórnej medicíny. - ISSN 1338-9661 . - Roč. 2 [6], č. 1 (2015), s. 7-10  : ilustr., fareb., graf, sch.  
    C 3151
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  9. 9.RASSF1A and CDH1 hypermethylation as potential epimarkers in breast cancer

    RASSF1A and CDH1 hypermethylation as potential epimarkers in breast cancer  / Sebova K. ... [et al.] .  Cancer Biomarkers . - vol. 10, no. 1 (2011/2012), s. 13-26   [Dokument nie je vo fonde knižnice]
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  10. 10.The most frequent APC mutations among Slovak familial adenomatous polyposis patients

    The most frequent APC mutations among Slovak familial adenomatous polyposis patients  / V. Zajac ... [e al.] .  Neoplasma : journal of experimental and clinical oncology. - ISSN 0028-2685 . - Roč. 49, č. 6 (2002), s. 356-361  : Grafy, obr., tab.  
    C 720
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