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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, Berna1 (AUTHOR), Donbaloğlu, Zeynep1 (AUTHOR), Çetiner, Ebru Barsal1 (AUTHOR), Bedel, Aynur1 (AUTHOR), Çetin, Kürşat1 (AUTHOR), Paksoy, Belgin Akcan2 (AUTHOR), Kalkan, Tarkan3 (AUTHOR), Akbaş, Halide4 (AUTHOR), Tuhan, Hale Ünver1 (AUTHOR), Parlak, Mesut1 (AUTHOR) mesutparlak@akdeniz.edu.tr
Source: Journal of Clinical Research in Pediatric Endocrinology. 2026 Suppl, Vol. 18, p83-91. 9p.
Database: Academic Search Ultimate
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PubType: Academic Journal
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  Data: Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder.
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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>. 2026 Suppl, Vol. 18, p83-91. 9p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=194179533
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        Value: 10.4274/jcrpe.galenos.2025.2024-12-4
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              Text: 2026 Suppl
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