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Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders.

Document Type

Article

Author

Wigby, Kristen M.; Brockman, Deanna; Costain, Gregory; Hale, Caitlin; Taylor, Stacie L.; Belmont, John; Bick, David; Dimmock, David; Fernbach, Susan; Greally, John; Jobanputra, Vaidehi; Kulkarni, Shashikant; Spiteri, Elizabeth; Taft, Ryan J.

Source

NPJ Genomic Medicine; 2/26/2024, Vol. 9 Issue 1, p1-11, 11p

Subject

Language

ISSN

20567944

Online Access

Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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