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A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation
| Title: | A New Case of Rare Microdeletion 10q22.3q23 along with Mosaic Klinefelter Syndrome Associated with Facial Dysmorphic Finding, Atrial Ventricular Septal Defect, and Motor Retardation | Authors: | Dincsoy, Bir Firdevs; Silan, Fatma; Velickovic, Jelena; Berkay, Akcan Mehmet; Ozdemir, Ozturk | Issue Date: | 2022 | Publication: | MOLECULAR SYNDROMOLOGY | ISSN: | 1661-8769 Molecular Syndromology Search Idenfier |
Type: | Article | Collation: | vol. 13 br. 3 str. 254-260 | DOI: | 10.1159/000519965 | WoS-ID: | 000753756300001 | Scopus-ID: | 2-s2.0-85124905802 | PMID: | 35707596 | PMCID: | PMC9149477 | URI: | https://enauka.gov.rs/handle/123456789/825328 | Project: | Scientific Research Foundation Unit (BAP) of Canakkale Onsekiz Mart University, Canakkale-Turkey [BAP-TAY2015/445] | Metadata source: | (Preuzeto iz Nasi u WoS) | M-category: | 23M23 |
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