Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder
Authors:
- Berna SinginBSBerna Singin
- Zeynep DonbaloğluZDZeynep Donbaloğlu
- Ebru Barsal ÇetinerEÇEbru Barsal Çetiner
- Aynur BedelABAynur Bedel
- Kürşat ÇetinKÇKürşat Çetin
- Belgin Akcan PaksoyBPBelgin Akcan Paksoy
- Tarkan KalkanTKTarkan Kalkan
- Halide AkbaşHAHalide Akbaş
- Hale Ünver TuhanHTHale Ünver Tuhan
- Mesut ParlakMPMesut Parlak
Open Access
- 19 March 2025
- journal article
- review article
- Published by Galenos Yayinevi in Journal of Clinical Research in Pediatric Endocrinology
- Vol. 18 (Suppl 1) , 83-91
Abstract
Xp21 Contiguous Gene Deletion Syndrome: Diagnosis, Treatment, and a Review of the Literature on a Rare Genetic Disorder - Journal of Clinical Research in Pediatric EndocrinologyKeywords
This publication has 31 references indexed in Scilit:
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