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Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting

Document Type

Article

Author

Mazzonetto, P.C.; da Costa, S.S.; Krepischi, A.C.V.; Rosenberg, C.; Villela, D.; Milanezi, F.; Migliavacca, M.P.; Pierry, P.M.; Bonaldi, A.; Almeida, L.G.D.; De Souza, C.A.; Kroll, J.E.; Paula, M.G.; Guarischi-Sousa, R.; Scapulatempo-Neto, C.

Source

In: Annals of Human Genetics. (Annals of Human Genetics, March 2024, 88(2):113-125)

Subject

Language

English

ISSN

14691809
00034800

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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