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A 39 kb structural variant causing Lynch Syndrome detected by optical genome mapping and nanopore sequencing

Document Type

Journal

Author

Bjornstad, Pal Marius; Aalokken, Ragnhild; Asheim, June; Sundaram, Arvind Y. M.; Felde, Caroline N.; Ostby, G. Henriette; Dalland, Marianne; Sjursen, Wenche; Carrizosa, Christian; Vigeland, Magnus D.; Sorte, Hanne S.; Sheng, Ying; Ariansen, Sarah L.; Grindedal, Eli Marie; Gilfillan, Gregor D.

Source

EUROPEAN JOURNAL OF HUMAN GENETICS; NOV 29 2023, 8p.

Subject

Language

English

ISSN

14765438

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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