Rezultati
eNauka >
Rezultati >
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
| Naziv: | 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 | Autori: | Dincsoy, Bir Firdevs; Silan, Fatma; Velickovic, Jelena; Berkay, Akcan Mehmet; Ozdemir, Ozturk | Godina: | 2022 | Publikacija: | MOLECULAR SYNDROMOLOGY | ISSN: | 1661-8769 Molecular Syndromology Pretraži identifikator |
Tip rezultata: | Naučni članak | Kolacija: | 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 | Projekat: | Scientific Research Foundation Unit (BAP) of Canakkale Onsekiz Mart University, Canakkale-Turkey [BAP-TAY2015/445] | Izvor metapodataka: | (Preuzeto iz Nasi u WoS) | M-kategorija: | 23M23 - Međunarodni časopis kategorije M23 |
Rezultati na eNauka su zaštićeni autorskim pravima i sva prava su zadržana, osim ako nije drugačije naznačeno.