Search Results - Özgür Çoğulu
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1
Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings by Esra Işık, Bilcağ Akgün, Tahir Atik, Ferda Özkınay, Özgür Çoğulu
Published 2020Call Number: Loading…Connect to this object online.
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2
The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals by Fatma E. Koku, Süleyman O. Karamızrak, Aynur S. Çiftçi, Hasan Taşlıdere, Burak Durmaz, Özgür Çoğulu
Published 2018Call Number: Loading…Connect to this object online.
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3
Aromatase Deficiency in Two Siblings with 46,XX Karyotype Raised as Different Genders: A Novel Mutation (p.R115X) in the CYP19A1 Gene by Samim Özen, Tahir Atik, Özlem Korkmaz, Hüseyin Onay, Damla Gökşen, Ferda Özkınay, Özgür Çoğulu, Şükran Darcan
Published 2020Call Number: Loading…Connect to this object online.
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4
Detection of <italic>SHOX</italic> Gene Variations in Patients with Skeletal Abnormalities with or without Short Stature by Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anıl Korkmaz, Korcan Demir, Behzat Özkan, Özgür Çoğulu
Published 2020Call Number: Loading…Connect to this object online.
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5
A Neurofibromatosis Noonan Syndrome Patient Presenting with Abnormal External Genitalia by Esra Işık, Hüseyin Onay, Tahir Atik, Aslı Ece Solmaz, Samim Özen, Özgür Çoğulu, Şükran Darcan, Ferda Özkınay
Published 2020Call Number: Loading…Connect to this object online.
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6
Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review by Gizem Kok Kilic, Erhan Pariltay, Emin Karaca, Burak Durmaz, Huseyin Ekici, Metehan Imamoglu, Firat Okmen, Haluk Akin, Ozgur Cogulu
Published 2022Call Number: Loading…Connect to this object online.
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7
Diagnostic yield of exome sequencing-based copy number variation analysis in Mendelian disorders: a clinical application by Tahir Atik, Enise Avci Durmusalioglu, Esra Isik, Melis Kose, Seda Kanmaz, Ayca Aykut, Asude Durmaz, Ferda Ozkinay, Ozgur Cogulu
Published 2024Call Number: Loading…Connect to this object online.
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8
A New Cause of Obesity Syndrome Associated with a Mutation in the Carboxypeptidase Gene Detected in Three Siblings with Obesity, Intellectual Disability and Hypogonadotropic Hypogo... by Asude Durmaz, Ayça Aykut, Tahir Atik, Samim Özen, Durdugül Ayyıldız Emecen, Aysun Ata, Esra Işık, Damla Gökşen, Özgür Çoğulu, Ferda Özkınay
Published 2021Call Number: Loading…Connect to this object online.
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9
Quality of Life and Psychological Well-being in Children and Adolescents with Disorders of Sex Development by Birsen Şentürk Pilan, Burcu Özbaran, Didem Çelik, Tuğçe Özcan, Samim Özen, Damla Gökşen, İbrahim Ulman, Ali Avanoğlu, Sibel Tiryaki, Hüseyin Onay, Özgür Çoğulu, Ferda Özkınay, Şükran Darcan
Published 2021Call Number: Loading…Connect to this object online.
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