De Novo Large Deletion Leading to Fragile X Syndrome

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dc.contributor.authorPoonnada Jiraanont
dc.contributor.authorEsther Manor
dc.contributor.authorNazi Tabatadze
dc.contributor.authorMarwa Zafarullah
dc.contributor.authorGuadalupe Mendoza
dc.contributor.authorGia Melikishvili
dc.contributor.authorFlora Tassone
dc.date.accessioned2026-05-08T19:17:57Z
dc.date.issued2022-5-11
dc.description.abstractthroughout the article).
dc.identifier.doi10.3389/fgene.2022.884424
dc.identifier.urihttps://dspace.kmitl.ac.th/handle/123456789/16289
dc.publisherFrontiers in Genetics
dc.subjectGenetics and Neurodevelopmental Disorders
dc.subjectGenomic variations and chromosomal abnormalities
dc.subjectCongenital heart defects research
dc.titleDe Novo Large Deletion Leading to Fragile X Syndrome
dc.typeArticle

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