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Germline CNV Detection through Whole-Exome Sequencing (WES) Data Analysis Enhances Resolution of Rare Genetic Diseases

Document Type

Article

Author

Tilemis, F.-N.; Marinakis, N.M.; Veltra, D.; Svingou, M.; Kekou, K.; Mitrakos, A.; Tzetis, M.; Kosma, K.; Makrythanasis, P.; Traeger-Synodinos, J.; Sofocleous, C.

Source

In: Genes. (Genes, July 2023, 14(7))

Subject

Language

English

ISSN

20734425

Online Access

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

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