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PCR based diagnosis of 21-hydroxylase gene defects in slovak patients with congenital adrenal hyperplasia

  1. TitlePCR based diagnosis of 21-hydroxylase gene defects in slovak patients with congenital adrenal hyperplasia
    Author Pinterová L.
    Co-authors Garami M.

    Pribilincová Zuzana

    Behulová R.

    Mezenská R.

    Lukáčová Magdaléna SAVVIR - Virologický ústav SAV

    Zorad Štefan SAVEXEND - Ústav experimentálnej endokrinológie SAV    SCOPUS    RID    ORCID

    Source document Endocrine Regulations. Vol. 34, no. 2 (2000), p. 65-72
    Languageeng - English
    Document kindrozpis článkov z periodík (rbx)
    CitationsAKHMETOVA, V.L. - RAMOVA, Z.F. - MALIEVSKY, O.A. - KHUSNUTDINOVA, E.K. Mutational spectrum of the gene for 21-hydroxylase in the patients with congenital adrenal hyperplasia from Bashkortostan. In Russian Journal of Genetics, 2008, vol.44, no.10, 1233-1240.
    CategoryADFB - Scientific papers in other domestic journals not registered in Current Contents Connect without IF (non-impacted)
    Category of document (from 2022)V3 - Vedecký výstup publikačnej činnosti z časopisu
    Type of documentčlánok
    Year2000
    Registered inSCOPUS
    article

    article

    rokCCIFIF Q (best)JCR Av Jour IF PercSJRSJR Q (best)CiteScore
    N
    rok vydaniarok metrikyIFIF Q (best)SJRSJR Q (best)
    2000
Number of the records: 1  

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