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A deep phenotyping experience: up to date in management and diagnosis of Malan syndrome in a single center surveillance report

Document Type

Article

Author

Macchiaiolo, M.; Vecchio, D.; Gonfiantini, M.V.; Cortellessa, F.; Bartuli, A.; Panfili, F.M.; Caciolo, C.; Alfieri, P.; Zollino, M.; Accadia, M.; Seri, M.; Chinali, M.; Mammì, C.; Priolo, M.; Tartaglia, M.

Source

In: Orphanet Journal of Rare Diseases. (Orphanet Journal of Rare Diseases, December 2022, 17(1))

Subject

Language

English

ISSN

17501172

Online Access

EBSCOHost PDF Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Open Access (BioMed Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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