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Article: Molecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone

TitleMolecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone
Authors
Issue Date2022
Citation
Clinica Chimica Acta, 2022, v. 524, p. 1-10 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/319908
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHe, D-
dc.contributor.authorLi, Y-
dc.contributor.authorYang, W-
dc.contributor.authorChen, S-
dc.contributor.authorSun, H-
dc.contributor.authorLi, P-
dc.contributor.authorZhang, M-
dc.contributor.authorBan, B-
dc.date.accessioned2022-10-14T05:21:57Z-
dc.date.available2022-10-14T05:21:57Z-
dc.date.issued2022-
dc.identifier.citationClinica Chimica Acta, 2022, v. 524, p. 1-10-
dc.identifier.urihttp://hdl.handle.net/10722/319908-
dc.languageeng-
dc.relation.ispartofClinica Chimica Acta-
dc.titleMolecular diagnosis for growth hormone deficiency in Chinese children and adolescents and evaluation of impact of rare genetic variants on treatment efficacy of growth hormone-
dc.typeArticle-
dc.identifier.emailYang, W: yangwl@hku.hk-
dc.identifier.authorityYang, W=rp00524-
dc.identifier.doi10.1016/j.cca.2021.11.021-
dc.identifier.hkuros339146-
dc.identifier.volume524-
dc.identifier.spage1-
dc.identifier.epage10-
dc.identifier.isiWOS:000790634000001-

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