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Material Type: Artigo
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Multidisciplinary Approach to Hypnosis: Psychiatric Basis, Neuroimaging and Genetic Findings: Hipnoza Multidisipliner Yaklasim: Psikiyatrik Temeli, Nörogörüntüleme ve Genetik BulgularOzsunar, Yelda ; Kayhan, Handan ; Ince, Lara UtkuPsikiyatride güncel yaklaşimlar, 2024-06, Vol.16 (3), p.451 [Periódico revisado por pares]Anadolu Psikiyatri DergisiTexto completo disponível |
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Material Type: Artigo
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Multidisciplinary Approach to Hypnosis: Psychiatric Basis, Neuroimaging and Genetic Findings: Hipnoza Multidisipliner Yaklasim: Psikiyatrik Temeli, Nörogörüntüleme ve Genetik BulgularOzsunar, Yelda ; Kayhan, Handan ; Ince, Lara UtkuPsikiyatride güncel yaklaşimlar, 2024-06, Vol.16 (3), p.451 [Periódico revisado por pares]Anadolu Psikiyatri DergisiTexto completo disponível |
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Material Type: Artigo
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A Report on Children with CEP290 Mutation, Vision Loss, and Developmental DelaySahli, EsraBeyoglu Eye Journal, 2023, Vol.8 (3), p.226-232 [Periódico revisado por pares]Turkey: Kare PublishingTexto completo disponível |
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Material Type: Artigo
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Genetic Causes of Inner Ear Anomalies: a Review from the Turkish Study Group for Inner Ear AnomaliesOcak, Emre ; Duman, Duygu ; Tekin, Mustafa Koçak,ZaferBalkan medical journal, 2019-07, Vol.36 (4), p.206-211 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Investigation of Catechol-O-Methyltransferase and Cannabinoid Receptor 2 gene variants in tobacco use disorder or tobacco use disorder and schizophrenia comorbidity/Tutun kullanim bozuklugu veya tutun kullanim bozuklugu ve sizofreni komorbiditesinde Katekol-O-Metiltransferaz ve Kannabinoid Reseptor 2 gen varyantlarinin incelenmesiPehlivan, Sacide ; Aydin, Pinar Cetinay ; Aytac, Hasan Mervan ; Uysal, Mehmet Atilla ; Sever, Ulgen ; Pehlivan, MustafaAnadolu psikiyatri dergisi, 2020-12, Vol.21 (6), p.572 [Periódico revisado por pares]Anadolu Psikiyatri DergisiTexto completo disponível |
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Material Type: Artigo
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Are COL4A1 and COL4A2 gene polymorphisms associated with cerebral palsy?Guvener, Orhan ; Sezgin, Melek ; Tezol, Ozlem ; Barlas, Ibrahim Omer ; Ozdemir, Asena Ayca ; Kanik, Emine ArzuTurkish journal of physical medicine and rehabilitation, 2021-06, Vol.67 (2), p.242-249 [Periódico revisado por pares]Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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FBLN 4 mutasyonuna bagli dev cikan aort anevrizmasi: olgu serisi/Giant aortic aneurysm due to fibulin- 4 deficiency: case seriesSulu, Ayse ; Baspmar, Osman ; Sahin, Derya AydinTurk Pediatri Arsivi, 2019-06, Vol.54 (2), p.119 [Periódico revisado por pares]AVESTexto completo disponível |
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Material Type: Artigo
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The importance of R202Q polymorphism in clinical expression of Familial Mediterranean FeverTekgoz, Emre ; Cinar, Fatma Ilknur ; Cinar, Muhammet ; Yilmaz, SedatGülhane tıp dergisi, 2020-09, Vol.62 (3), p.157-162 [Periódico revisado por pares]Ankara: Galenos Yayinevi Tic. LtdTexto completo disponível |
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Material Type: Artigo
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Tryptophan hydroxylase gene polymorphism in patients with obsessive-compulsive disorder/Obsesif kompulsif bozukluk hastalarinda triptofanhidroksilaz gen polimorfizmiKorkmaz, Sevda ; Onalan, Ebru ; Yuce, Huseyin ; Atmaca, MuradAnadolu psikiyatri dergisi, 2016-04, Vol.17 (2), p.85 [Periódico revisado por pares]Anadolu Psikiyatri DergisiTexto completo disponível |
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Material Type: Artigo
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Inherited Deletion of 1q, Hyperparathyroidism and Signs of Y-chromosomal Influence in a Patient with Turner SyndromeSiller, Alejandro F. ; Shimony, Alex ; Shinawi, Marwan ; Amarillo, Ina ; Dehner, Louis P. ; Semenkovich, Katherine ; Arbeláez, Ana María Darendeliler,Fatma FeyzaJournal of clinical research in pediatric endocrinology, 2019-03, Vol.11 (1), p.88-93 [Periódico revisado por pares]Turkey: Galenos Yayinevi Tic. LtdTexto completo disponível |