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MKS1 mutations cause Joubert syndrome with agenesis of the corpus callosum

Document Type

Article

Author

Bader, Ingrid; Decker, E.; Mayr, J.A.; Lunzer, V.; Koch, J.; Boltshauser, E.; Sperl, W.; Pietsch, P.; Ertl-Wagner, B.; Bolz, H.; Bergmann, C.; Rittinger, O.

Source

In European Journal of Medical Genetics August 2016 59(8):386-391

Subject

Language

ISSN

1769-7212

Online Access

Full Text (ScienceDirect 종량제) Full Text (Clinical Key) Web of Science JCR 저널정보 Scopus Find it@PNU

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