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SPECC1L Mutations Are Not Common in Sporadic Cases of Opitz G/BBB Syndrome

Document Type

Journal

Author

Migliore, Chiara; Vendramin, Anna; McKee, Shane; Prontera, Paolo; Faravelli, Francesca; Sachdev, Rani; Dias, Patricia; Mascaro, Martina; Licastro, Danilo; Meroni, Germana

Source

GENES; FEB 2022, 13 2, p252 10p.

Subject

Language

English

ISSN

20734425

Online Access

Full Text (ProQuest Central) Full Text (Gale Academic Onefile) Web of Science JCR 저널정보 Scopus Find it@PNU

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