Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders.

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Title: Structural Variant and Repeat Expansion Findings Identified by Optical Genome Mapping in Complex Autism Spectrum Disorder With Concomitant Neurodevelopmental Disorders.
Authors: Mutlu MB; Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Öğütlü ÖBG; Department of Medical Genetics, Erzurum Regional Training and Research Hospital, Erzurum, Türkiye, erzurumbeah.gov.tr., Öz Ö; Department of Medical Genetics, Harran University Faculty of Medicine, Şanlıurfa, Türkiye, harran.edu.tr., Duymuş F; Department of Medical Genetics, Uşak University, Faculty of Medicine, Uşak, Türkiye, usak.edu.tr., Seyhan S; Medroyal Genetic Diseases Assessment Center, İstanbul, Türkiye., Tokaç AGB; Department of Internal Medicine, Division of Medical Genetics, İstanbul University, Faculty of Medicine, İstanbul, Türkiye, istanbul.edu.tr., Tezcan E; Department of Child and Adolescent Psychiatry, Selçuk University, Faculty of Medicine, Konya, Türkiye, selcuk.edu.tr., Öğütlü H; Department of Child and Adolescent Psychiatry, University College Dublin, Dublin, Ireland, ucd.ie., Demiryılmaz F; Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Silahtarlıoğlu N; Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Bilgil K; Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Elma S; Detagen Genetic Diseases Evaluation Center, Kayseri, Türkiye., Erdoğan M; Department of Medical Genetics, University of Health Science, Kayseri Faculty of Medicine, Kayseri, Türkiye, sbu.edu.tr., Gümüş H; Department of Pediatrics, Division of Pediatric Neurology, Erciyes University, Faculty of Medicine, Kayseri, Türkiye, erciyes.edu.tr., Kumandaş S; Department of Pediatrics, Division of Pediatric Neurology, Erciyes University, Faculty of Medicine, Kayseri, Türkiye, erciyes.edu.tr., Kılıçaslan F; Department of Child and Adolescent Psychiatry, Harran University, Faculty of Medicine, Şanlıurfa, Türkiye, harran.edu.tr.
Source: Human mutation [Hum Mutat] 2026 Jun 11; Vol. 2026, pp. 3130383. Date of Electronic Publication: 2026 Jun 11 (Print Publication: 2026).
Publication Type: Journal Article
Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1098-1004
DOI:10.1155/humu/3130383