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Missed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome

DC FieldValueLanguage
dc.contributor.author이승태-
dc.contributor.author한진우-
dc.date.accessioned2020-02-26T06:33:31Z-
dc.date.available2020-02-26T06:33:31Z-
dc.date.issued2019-
dc.identifier.issn2168-6165-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/175197-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherAmerican Medical Association-
dc.relation.isPartOfJAMA OPHTHALMOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleMissed Heterozygous Deletion in Study of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Laboratory Medicine (진단검사의학교실)-
dc.contributor.googleauthorSeung-Tae Lee-
dc.contributor.googleauthorJinu Han-
dc.identifier.doi10.1001/jamaophthalmol.2019.3755-
dc.contributor.localIdA04627-
dc.contributor.localIdA04329-
dc.contributor.localIdA04329-
dc.relation.journalcodeJ01200-
dc.identifier.eissn2168-6173-
dc.contributor.alternativeNameLee, Seung-Tae-
dc.contributor.affiliatedAuthor이승태-
dc.contributor.affiliatedAuthor한진우-
dc.contributor.affiliatedAuthor한진우-
dc.citation.volume137-
dc.citation.number12-
dc.citation.startPage1465-
dc.citation.endPage1466-
dc.identifier.bibliographicCitationJAMA OPHTHALMOLOGY, Vol.137(12) : 1465-1466, 2019-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Laboratory Medicine (진단검사의학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Ophthalmology (안과학교실) > 1. Journal Papers

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