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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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Bibliographic Details
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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Description
ISSN:13085727
DOI:10.4274/jcrpe.galenos.2025.2025-1-18