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1دورية أكاديمية
المؤلفون: Aslı Derya Kardelen, Adam Najaflı, Firdevs Baş, Birsen Karaman, Güven Toksoy, Şükran Poyrazoğlu, Şahin Avcı, Umut Altunoğlu, Zehra Yavaş Abalı, Ayşe Pınar Öztürk, Esin Karakılıç Özturan, Seher Başaran, Feyza Darendeliler, Z. Oya Uyguner
المصدر: JCRPE, Vol 15, Iss 4, Pp 338-347 (2023)
مصطلحات موضوعية: growth hormone deficiency, multiple pituitary hormone deficiency, prokr2, short stature, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Yeliz Guven, Hilal Piril Saracoglu, Sermin Dicle Aksakal, Tugba Kalayci, Umut Altunoglu, Zehra Oya Uyguner, Serpil Eraslan, Esra Borklu, Hulya Kayserili
المصدر: BMC Oral Health, Vol 23, Iss 1, Pp 1-9 (2023)
مصطلحات موضوعية: Nance–Horan syndrome, Cataracts and teeth anomalies, Hutchinson teeth, Bud-shaped molars, Screwdriver shaped incisors, Supernumerary teeth, Dentistry, RK1-715
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1472-6831
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3دورية أكاديمية
المؤلفون: Asuman Gedikbasi, Guven Toksoy, Meryem Karaca, Cagri Gulec, Mehmet Cihan Balci, Dilek Gunes, Seda Gunes, Ayca Dilruba Aslanger, Gokcen Unverengil, Birsen Karaman, Seher Basaran, Mubeccel Demirkol, Gulden Fatma Gokcay, Zehra Oya Uyguner
المصدر: Frontiers in Genetics, Vol 14 (2023)
مصطلحات موضوعية: mitochondrial diseases, mtDNA, bi-genomic sequencing, exome sequencing, differential diagnosis, Genetics, QH426-470
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Neşe Akcan, Oya Uyguner, Firdevs Baş, Umut Altunoğlu, Güven Toksoy, Birsen Karaman, Şahin Avcı, Zehra Yavaş Abalı, Şükran Poyrazoğlu, Agharza Aghayev, Volkan Karaman, Rüveyde Bundak, Seher Başaran, Feyza Darendeliler
المصدر: JCRPE, Vol 14, Iss 2, Pp 153-171 (2022)
مصطلحات موضوعية: 46, xy disorders of sex development, 5α, -reductase deficiency, androgen insensitivity syndrome, androgen receptor gene mutations, srd5a2 gene mutations, Pediatrics, RJ1-570, Diseases of the endocrine glands. Clinical endocrinology, RC648-665
وصف الملف: electronic resource
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5دورية أكاديمية
المؤلفون: Burcu Sevinç Rüstemoğlu, Bedia Samanci, Fatih Tepgeç, Murat Kürtüncü, Umut Altunoglu, Tuncay Gündüz, Gözde Yeşil, Şahin Avcı, Hakan Gürvit, Başar Bilgiç, Güven Toksoy, Mefkure Eraksoy, Haşmet Hanağası, Zehra Oya Uyguner
المصدر: Türk Nöroloji Dergisi, Vol 27, Iss 3, Pp 240-247 (2021)
مصطلحات موضوعية: carasil, cadasil, autosomal dominant, recessive, notch3, htra1, Medicine, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
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6دورية أكاديمية
المؤلفون: Mustafa Bilici, Serap Karaman, Aysegul Unuvar, Deniz Tugcu, Gülsah Tanyildiz, Ayca Dilruba Aslanger, Oya Uyguner, Rumeysa Tuna Deveci, Sifa Sahin, Zeynep Karakas
المصدر: Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S62-S63 (2021)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
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7دورية أكاديمية
المؤلفون: Yavas Abali, Zehra, Gokpinar Ili, Ezgi, Bas, Firdevs, Ulak Ozkan, Melis, Gulec, Çagrı, Toksoy, Guven, Ozturk, Ayşe Pinar, Karakilic Ozturan, Esin, Aslanger, Ayça, Caliskan, Mine, Yesil, Gozde, Poyrazoglu, Sukran, Darendeliler, Feyza, Oya Uyguner, Zehra
المصدر: Hormone Research in Paediatrics; 2024, Vol. 97 Issue 2, p157-164, 8p
مصطلحات موضوعية: HYPOPITUITARISM, GENETIC variation, NEUROPATHY, HORMONE deficiencies, PITUITARY dwarfism, PHENOTYPES
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8
المؤلفون: G. Tutku Turgut, Ibrahim Halil Kalelioglu, Volkan Karaman, Tugba Sarac Sivrikoz, Birsen Karaman, Zehra Oya Uyguner, Tugba Kalayci
المصدر: Molecular Syndromology. 14:152-157
مصطلحات موضوعية: Genetics, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::00a17eeebae6b8f2d8f1029785b7a277
https://doi.org/10.1159/000527955 -
9دورية أكاديمية
المؤلفون: Birsen Karaman, Hülya Kayserili, Asadollah Ghanbari, Zehra Oya Uyguner, Güven Toksoy, Umut Altunoglu, Seher Basaran
المصدر: Molecular Cytogenetics, Vol 11, Iss 1, Pp 1-7 (2018)
مصطلحات موضوعية: OMIM 601803, Pallister-Killian syndrome, Somatic mosaicism, Mosaic tetrasomy 12p, Isochromosome 12p, Parental origin, Genetics, QH426-470
وصف الملف: electronic resource
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10دورية أكاديمية
المؤلفون: Fahrettin Uysal, Burcu Turkgenc, Guven Toksoy, Ozlem M. Bostan, Elif Evke, Oya Uyguner, Cengiz Yakicier, Hulya Kayserili, Ergun Cil, Sehime G. Temel
المصدر: BMC Medical Genetics, Vol 18, Iss 1, Pp 1-8 (2017)
مصطلحات موضوعية: Jervell-Lange-Nielsen syndrome, Deafness, Homozygous or compound heterozygous mutations, Case report, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource