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eNauka >  Rezultati >  The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
Naziv: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
Autori: Pignatelli, Duarte; Carvalho, Berta L.; Palmeiro, Aida; Barros, Alberto; Guerreiro, Susana G.; Macut,Đuro P.  
Godina: 2019
Publikacija: Frontiers in endocrinology
ISSN: 1664-2392 Frontiers in Endocrinology Pretraži identifikator
Izdavač: [Lausanne : Frontiers Research Foundation]
Tip rezultata: Naučni članak
Kolacija: vol. 10 str. 432
DOI: 10.3389/fendo.2019.00432
WoS-ID: 000474257500001
Scopus-ID: 2-s2.0-85069452448
PMID: 31333583
PMCID: PMC6620563
URI: https://enauka.gov.rs/handle/123456789/814301
URL: https://www.frontiersin.org/journals/endocrinology/articles/10.3389/fendo.2019.00432/full
Projekat: Foundation for Science and Technology (FCT) [PTDC/MEC-ONC/31384/2017]
FCT [SFRH/BPD/1117441/2015]
Izvor metapodataka: (Preuzeto iz Nasi u WoS)
M-kategorija: 
21M21 - Vodeći međunarodni časopis kategorije M21

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