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SCIP: software for efficient clinical interpretation of copy number variants detected by whole-genome sequencing

Document Type

Article

Author

Ding, Q.; Somerville, C.; Manshaei, R.; Kalbfleisch, K.; Stanley, K.; Okello, J.B.A.; Hosseini, S.M.; Liston, E.; Curtis, M.; Kim, R.H.; Jobling, R.K.; Trost, B.; Reuter, M.S.; Zarrei, M.; Higginbotham, E.J.; Chan, A.J.S.; Engchuan, W.; Thiruvahindrapuram, B.; Scherer, S.W.

Source

In: Human Genetics. (Human Genetics, February 2023, 142(2):201-216)

Subject

Language

English

ISSN

14321203
03406717

Online Access

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

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