Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder

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Title: Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder
Authors: Singin B; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Donbaloğlu Z; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Barsal Çetiner E; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Bedel A; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Çetin K; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Akcan Paksoy B; Akdeniz University Faculty of Medicine, Department of Pediatric Metabolic Diseases, Antalya, Türkiye, Kalkan T; University of Health Sciences Türkiye, Antalya Training and Research Hospital, Clinic of Molecular Genetics, Antalya, Türkiye, Akbaş H; Akdeniz University Faculty of Medicine, Department of Medical Biochemistry, Antalya, Türkiye, Ünver Tuhan H; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye, Parlak M; Akdeniz University Faculty of Medicine, Department of Pediatric Endocrinology, Antalya, Türkiye
Source: Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2026 May 22; Vol. 18 (Suppl 1), pp. 83-91. Date of Electronic Publication: 2025 Mar 19.
Publication Type: Journal Article; Case Reports; Review
Journal Info: Publisher: Galenos Yayınevi Country of Publication: Turkey NLM ID: 101519456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1308-5735 (Electronic) NLM ISO Abbreviation: J Clin Res Pediatr Endocrinol Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1308-5735
DOI:10.4274/jcrpe.galenos.2025.2024-12-4