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High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey

Document Type

Academic Journal

Author

Kalb, S; Caglayan, A O; Degerliyurt, A; Schmid, S; Ceylaner, S; Hatipoglu, N; Hinderhofer, K; Rehder, H; Kurtoglu, S; Ceylaner, G; Zschocke, J; Witsch-Baumgartner, M

Source

Clinical Genetics. Jun 01, 2012 81(6):598-601

Subject

Language

English

ISSN

0009-9163

Online Access

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

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