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NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families

Document Type

Article

Author

Al Shehhi, Maryam; Forman, Eva B.; Fitzgerald, Jacqueline E.; McInerney, Veronica; Krawczyk, Janusz; Shen, Sanbing; Betts, David R.; Ardle, Linda Mc; Gorman, Kathleen M.; King, Mary D.; Green, Andrew; Gallagher, Louise; Lynch, Sally A.

Source

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

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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