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PCR based diagnosis of 21-hydroxylase gene defects in slovak patients with congenital adrenal hyperplasia
Title PCR 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 Language eng - English Document kind rozpis článkov z periodík (rbx) Citations AKHMETOVA, 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. Category ADFB - 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 document článok Year 2000 Registered in SCOPUS article
rok CC IF IF Q (best) JCR Av Jour IF Perc SJR SJR Q (best) CiteScore N rok vydania rok metriky IF IF Q (best) SJR SJR Q (best) 2000
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