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NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

Document Type

Article

Author

Al Shehhi, M.; Betts, D.R.; Ardle, L.M.; Green, A.; Lynch, S.A.; Forman, E.B.; Gorman, K.M.; King, M.D.; Fitzgerald, J.E.; Gallagher, L.; McInerney, V.; Krawczyk, J.; Shen, S.

Source

In: European Journal of Medical Genetics. (European Journal of Medical Genetics, March 2019, 62(3):204-209)

Subject

Language

English

ISSN

18780849
17697212

Online Access

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

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