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Diagnostic Utility of Next-Generation Sequencing-based CNV Analysis in Eleven Patients with Peters-Plus Syndrome: A Single-Center Experience.

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Title: Diagnostic Utility of Next-Generation Sequencing-based CNV Analysis in Eleven Patients with Peters-Plus Syndrome: A Single-Center Experience.
Authors: Akalın, Akçahan1 (AUTHOR), Durmuşalioğlu, Enise Avcı2 (AUTHOR) eniseavci.ea@gmail.com, Özalkak, Şervan3 (AUTHOR), Yıldırım, Ruken3 (AUTHOR), Öz, Veysel4 (AUTHOR), Ünal, Edip5 (AUTHOR), Hazar, Leyla6 (AUTHOR), Tan, Türkan Turkut2 (AUTHOR), Doğan, Yusuf Can2 (AUTHOR), Atik, Tahir2 (AUTHOR), Çoğulu, Özgür2 (AUTHOR), Işık, Esra2 (AUTHOR)
Source: Journal of Clinical Research in Pediatric Endocrinology. Dec2025, Vol. 17 Issue 4, p436-448. 13p.
Database: Academic Search Ultimate
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  Data: Diagnostic Utility of Next-Generation Sequencing-based CNV Analysis in Eleven Patients with Peters-Plus Syndrome: A Single-Center Experience.
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Clinical+Research+in+Pediatric+Endocrinology%22">Journal of Clinical Research in Pediatric Endocrinology</searchLink>. Dec2025, Vol. 17 Issue 4, p436-448. 13p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=190169177
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        Value: 10.4274/jcrpe.galenos.2025.2025-1-18
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        Text: English
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      – TitleFull: Diagnostic Utility of Next-Generation Sequencing-based CNV Analysis in Eleven Patients with Peters-Plus Syndrome: A Single-Center Experience.
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              M: 12
              Text: Dec2025
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              Y: 2025
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