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Records found: 12  
Your query: Author Sysno/Doc.kind = "^sllk_un_auth p0044685 xaec^"

  1. 1.Effect of unexpected sequence interruptions to conventional PCR and repeat primed PCR in myotonic dystrophy type 1 testing

    Effect of unexpected sequence interruptions to conventional PCR and repeat primed PCR in myotonic dystrophy type 1 testing  / Radvanszky J, Ficek A, Minarik G, et al. .  Diagnostic molecular pathology . - vol. 20, no. 1 (2011), s. 48-51   [Dokument nie je vo fonde knižnice]
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  2. 2.High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)

    High frequency of GJB2 mutation W24X among Slovak Romany (Gypsy) patients with non-syndromic hearing loss (NSHL)  / G. Minárik ... [et al.] .  General physiology and biophysics : an international journal. - ISSN 0231-5882 . - Vol. 22, no. 4 (2003), p.549-556  : Grafy, obr., tab.  
    C 2357
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  3. 3.Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia

    Identification of the deletions in the UGT1A1 gene of the patients with Crigler-Najjar syndrome type I from Slovakia  / Zmetáková I. ... [et al.] .  General physiology and biophysics : an international journal. - ISSN 0231-5882 . - Vol. 26, no. 4 (2007), s. 306-310  
    C 2357
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  4. 4.Identifikácia a charakterizácia génu zodpovedného za vznik retinálnej degenerácie častej u slovenských Rómov

    Identifikácia a charakterizácia génu zodpovedného za vznik retinálnej degenerácie častej u slovenských Rómov  / A. Ficek ... [et al.] .  Časopis lékařů českých. - ISSN 0008-7335 . - Roč. 142, č. 5 (2003), s. 316  
    C 536
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  5. 5.Komplexná mutačná analýza génu PAH u slovenských pacientov postihnutých fenylketonúriou

    Komplexná mutačná analýza génu PAH u slovenských pacientov postihnutých fenylketonúriou  / E. Polák ... [et al.] .  Česko-slovenská pediatrie. - ISSN 0069-2328 . - Roč. 63, č. 10 (2008), s. 528-534  : ilustr., tab.  
    C 236
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  6. 6.Molekulová diagnostika dedičných nekonjugovaných hyperbilirubinémií na Slovensku

    Molekulová diagnostika dedičných nekonjugovaných hyperbilirubinémií na Slovensku  / Zmetáková I. ... [et al.] .  Česko-slovenská pediatrie. - ISSN 0069-2328 . - Roč. 64, č. 5 (2009), s. 223-229  : ilustr., obr.  
    C 236
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  7. 7.Phenylalanine hydroxylase deficiency in the Slovak population: genotype-phenotype correlations and genotype-based predictions of BH4-responsiveness

    Phenylalanine hydroxylase deficiency in the Slovak population: genotype-phenotype correlations and genotype-based predictions of BH4-responsiveness  / Polak E, Ficek A, Radvanszky J .  Gene . - Vol. 526, č. 2 - sept. 10 (2013), s. 347-355   [Dokument nie je vo fonde knižnice]
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  8. 8.Polymorphisms in genes involved in testosterone metabolism in Slovak autistic boys

    Polymorphisms in genes involved in testosterone metabolism in Slovak autistic boys  / Schmidtova E ... [et al.] .  The Endocrinologist . - Vol. 20, no. 5, (2010), pp. 245-249   [Dokument nie je vo fonde knižnice]
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  9. 9.Polymorphisms of candidate genes in Slovak autistic patients

    Polymorphisms of candidate genes in Slovak autistic patients  / Kelemenová S ... [et al.] .  Psychiatric genetics . - 20 (2010), pp. 137-139   [Dokument nie je vo fonde knižnice]
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  10. 10.Repeat-primed polymerase chain reaction in myotonic dystrophy type 2 testing

    Repeat-primed polymerase chain reaction in myotonic dystrophy type 2 testing  / Radvanszky J, Ficek A, Kadasi L .  Genetic testing and molecular biomarkers . - Vol. 15, no.3 (2011, s. 133-136   [Dokument nie je vo fonde knižnice]
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