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13q deletion syndrome involving rb1: Characterization of a new minimal critical region for psychomotor delay

Document Type

Article

Author

Privitera, F.; Doddato, G.; Papa, F.T.; Baldassarri, M.; Mari, F.; Renieri, A.; Ariani, F.; Calonaci, A.; Caini, M.; Galimberti, D.; Pinto, A.M.; Longo, I.; Hadjistilianou, T.; De Francesco, S.

Source

In: Genes. (Genes, September 2021, 12(9))

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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