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Evaluation of 100 Dutch cases with 16p11.2 deletion and duplication syndromes; from clinical manifestations towards personalized treatment options

Document Type

Journal

Author

Vos, Niels; Kleinendorst, Lotte; van der Laan, Liselot; van Uhm, Jorrit; Jansen, Philip R.; van Eeghen, Agnies M.; Maas, Saskia M.; Mannens, Marcel M. A. M.; van Haelst, Mieke M.

Source

EUROPEAN JOURNAL OF HUMAN GENETICS; APR 11 2024, 15p.

Subject

Language

English

ISSN

14765438

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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