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Eda Utine

Showing results (1-10 of 155) with videos related to

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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 Utine
The Turkish Journal of Pediatrics|November 7, 2013
A case of Sotos syndrome with 5q35 microdeletion and novel clinical findingsEsra Kılıç, Gülen Eda Utine, Koray Boduroğlu
Turkish Journal of Ophthalmology|January 5, 2017
A Baseline Algorithm for Molecular Diagnosis of Genetic Eye Diseases: Ophthalmologist's PerspectiveHande Taylan Şekeroğlu, Gülen Eda Utine, Mehmet Alikaşifoğlu
The Turkish Journal of Pediatrics|March 3, 2023
The Türkiye-Syria Earthquake: a response from the editors of the Turkish Journal of PediatricsAli Düzova, Sinem Akgül, Gülen Eda Utine, et al.
Journal of Child Neurology|January 27, 2016
A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson SyndromeEsra Kilic, Arda Cetinkaya, Gülen Eda Utine, et al.
European Journal of Medical Genetics|February 14, 2006
Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogueG Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, et al.
Ophthalmic Genetics|July 10, 2013
A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphylomaBerçin Tarlan, Hayyam Kiratli, Esra Kılıç, et al.
Clinical Dysmorphology|November 4, 2008
Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndromeMurat Kadri Erdoğan, Gülen Eda Utine, Yasemin Alanay, et al.
Clinical Dysmorphology|March 27, 2014
Prenatal diagnosis in a fetus with de-novo 20q11.2q13.1 deletion and review of the literatureMert Turgal, Ozgur Ozyuncu, G Eda Utine, et al.
Molecular Syndromology|February 6, 2025
A Case of Opsismodysplasia with a Novel <i>INPPL1</i> VariantTuğba Daşar, Ebru Aypar, Gülen Eda Utine, et al.
Pageof 16

Showing results (1-10 of 155) with videos related to

Sort By:
Pageof 16
Turkish Journal of Ophthalmology|May 6, 2021
Congenital Cataract and Its Genetics: The Era of Next-Generation SequencingHande Taylan Şekeroğlu, Gülen Eda Utine
The Turkish Journal of Pediatrics|November 7, 2013
A case of Sotos syndrome with 5q35 microdeletion and novel clinical findingsEsra Kılıç, Gülen Eda Utine, Koray Boduroğlu
Turkish Journal of Ophthalmology|January 5, 2017
A Baseline Algorithm for Molecular Diagnosis of Genetic Eye Diseases: Ophthalmologist's PerspectiveHande Taylan Şekeroğlu, Gülen Eda Utine, Mehmet Alikaşifoğlu
The Turkish Journal of Pediatrics|March 3, 2023
The Türkiye-Syria Earthquake: a response from the editors of the Turkish Journal of PediatricsAli Düzova, Sinem Akgül, Gülen Eda Utine, et al.
Journal of Child Neurology|January 27, 2016
A Diagnosis to Consider in Intellectual Disability: Mowat-Wilson SyndromeEsra Kilic, Arda Cetinkaya, Gülen Eda Utine, et al.
European Journal of Medical Genetics|February 14, 2006
Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogueG Eda Utine, Ayfer Alikasifoglu, Mehmet Alikasifoglu, et al.
Ophthalmic Genetics|July 10, 2013
A case of 22q11.2 deletion syndrome with right microphthalmia and left corneal staphylomaBerçin Tarlan, Hayyam Kiratli, Esra Kılıç, et al.
Clinical Dysmorphology|November 4, 2008
Unilateral Peters' anomaly in an infant with 22q11.2 deletion syndromeMurat Kadri Erdoğan, Gülen Eda Utine, Yasemin Alanay, et al.
Clinical Dysmorphology|March 27, 2014
Prenatal diagnosis in a fetus with de-novo 20q11.2q13.1 deletion and review of the literatureMert Turgal, Ozgur Ozyuncu, G Eda Utine, et al.
Molecular Syndromology|February 6, 2025
A Case of Opsismodysplasia with a Novel <i>INPPL1</i> VariantTuğba Daşar, Ebru Aypar, Gülen Eda Utine, et al.
Pageof 16