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Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia

Document Type

Article

Author

Barraza-García, J.; Rivera-Pedroza, C.I.; Hisado-Oliva, A.; Belinchón-Martínez, A.; Sentchordi-Montané, L.; del Pozo, A.; Ibáñez-Garikano, K.; Heath, K.E.; Duncan, E.L.; Clark, G.R.; Offiah, A.; Prieto-Matos, P.; Cormier-Daire, V.

Source

In: Clinical Genetics. (Clinical Genetics, July 2017, 92(1):91-98)

Subject

Language

English

ISSN

13990004
00099163

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Scopus Find it@PNU

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