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Turkish Journal of Ophthalmology|May 6, 2021
Congenital Cataract and Its Genetics: The Era of Next-Generation SequencingHande Taylan Şekeroğlu, Gülen Eda UtineThe Turkish Journal of Pediatrics|November 7, 2013
A case of Sotos syndrome with 5q35 microdeletion and novel clinical findingsEsra Kılıç, Gülen Eda Utine, Koray BoduroğluJournal of Child Neurology|January 27, 2016
A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson SyndromeEsra Kilic, Arda Cetinkaya, Gülen Eda Utine, et al.Molecular Syndromology|February 6, 2025
A Case of Opsismodysplasia with a Novel INPPL1 VariantTuğba Daşar, Ebru Aypar, Gülen Eda Utine, et al.European Journal of Medical Genetics|January 28, 2024
A spectrum of TP63-related disorders with eight affected individuals in five unrelated familiesMerve Soğukpınar, Gülen Eda Utine, Koray Boduroğlu, et al.American Journal of Medical Genetics. Part A|August 12, 2011
Catel-Manzke syndrome: a clinical report suggesting autosomal recessive inheritancePelin Özlem Şimşek Kiper, Gülen Eda Utine, Koray Boduroğlu, et al.The Turkish Journal of Pediatrics|August 20, 2010
Cowden syndrome with bronchial asthmaYasemin Ozsürekci, Süleyman Tolga Yavuz, Yasemin Alanay, et al.The Turkish Journal of Pediatrics|August 14, 2018
Anauxetic dysplasia: A rare clinical entityÖzlem Akgün-Doğan, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, et al.European Journal of Medical Genetics|April 28, 2021
Three new cases of Crisponi /cold induced sweating syndrome (CS/CISS1) in Turkish familiesAbdulkerim Kolkiran, Gizem Ürel-Demir, Pelin Özlem Şimşek-Kiper, et al.Molecular Syndromology|August 12, 2024
A Novel ZBTB20 Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive FeaturesMerve Soğukpınar, Beren Karaosmanoğlu, Gülen Eda Utine, et al.Pageof 7