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Birth Defects Research|July 12, 2025
Microarray Application in Newborns With Multiple Congenital Anomalies: Genotype-Phenotype CorrelationRamazan Keçeci, Hayriye Nermin Keçeci, Müşerref BaşdemirciMolecular Syndromology|May 13, 2026
Syndromic Alobar Holoprosencephaly Associated with a de novo 2p21p16.2 Contiguous Gene Deletion: A Neonatal Case ReportRamazan Keçeci, Hayriye Nermin Keçeci, Melek Büyükeren, et al.Birth Defects Research|March 27, 2020
Clinical characteristics and neonatal outcomes of liveborn newborns with hydrops fetalis treated in a tertiary level neonatal intensive care unitNuriye Emiroğlu, Fatma Hilal Yılmaz, Ramazan Keçeci, et al.Journal of Clinical Medicine|March 28, 2026
Long-Term Neurodevelopmental Outcomes and Prognostic Factors in Neonates with Hypoxic-Ischemic EncephalopathyRamazan Keçeci, Melek Büyükeren, Fatma Hilal Yılmaz, et al.Molecular Syndromology|October 9, 2025
Familial Hyperekplexia Caused by a Novel Homozygous SLC6A5 Variant: A Case ReportFatma Hilal Yılmaz, Ayça Burcu Kahraman, Fahrettin Duymuş, et al.Birth Defects Research|January 11, 2021
Is there a relationship between causative microorganisms and hearing loss in neonatal sepsis?Fatma Hilal Yilmaz, Nuriye Emiroğlu, Mehmet Burhan Oflaz, et al.Pageof 1