Vacuolated Leukocytes in the Peripheral Blood Smear of a Child with Chanarin-Dorfman Syndrome von Akyay, Arzu, Demir Şahin, Filiz, Şen, Aşkın

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Distinct Autism Spectrum Disorder Phenotype and Hand-Flapping Stereotypes: Two Siblings with Novel Homozygous Mutation in TRAPPC9 Gene and Literature Review von Bolat, Hilmi, Ünsel-Bolat, Gül, Derin, Hatice, Şen, Aşkın, Ceylaner, Serdar

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A family with interleukin-17 receptor A deficiency: a case report and review of the literature von Kilic, Mehmet, Ozcan, Mehmet Hazar, Taskin, Erdal, Sen, Askin

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Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation von Cimbek, Emine Ayça, Şen, Yaşar, Şen, Aşkın, Yuca, Sevil Arı, Buğrul, Fuat

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Prenatal Cytogenetic Findings in 13.466 Cases of High-Risk Pregnant Women in One Laboratory von Leyla Özer, Evrim Ünsal, Özge Ayvaz, Aşkın Şen, Volkan Baltacı

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Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium von Chawner, Samuel J.R.A., Mihaljevic, Marina, Morrison, Sinead, Eser, Hale Yapici, Maillard, Anne M., Nowakowska, Beata, van den Bree, Marianne B.M., Swillen, Ann

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Oculocutaneous Albinism Type 7 with Recurrent Infections: A Case Report von Kılıç, Mehmet, Özcan, Mehmet Hazar, Taskın, Erdal, Yıldırım, Hakan, Şen, Aşkın

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The Second and Third Hemoglobin Kansas Cases in the Turkish Population von Kayra Tanrıverdi, Zeynep, Akyay, Arzu, Şen, Aşkın, Taşkapan, Çağatay, Özgen, Ünsal

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The Vitamin D Receptor Gene Polymorphisms in Asthmatic Children: A Case-Control Study von Kilic, Mehmet, Ecin, Sema, Taskin, Erdal, Sen, Askin, Kara, Murat

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Kostmann Sendromu: Bir Vaka Sunumu von KILIÇ, Mehmet, ÖZCAN, Mehmet, TAŞKIN, Erdal, HÜZ, Zeynep, AKARSU, Saadet, ŞEN, Aşkın

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Evaluation of Clinical and Laboratory Features of Patients with Ataxia-Telangiectasia von KILIC, Mehmet, GUNBEY, Omer, TASKIN, Erdal, DAG, Bunyamin, KUCUK, Elif, GUNBEY, Fatma Betul, SEN, Askin

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A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation von Unal, Edip, Yıldırım, Ruken, Taş, Funda Feryal, Tekin, Suat, Sen, Askin, Haspolat, Yusuf Kenan

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Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation von Cimbek, Emine Ayca, Sen, Yasar, Sen, Askin, Yuca, Sevil Ari, Bugrul, Fuat

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Pseudohypoparathyroisidm Type 1a: A Case Report von Dogan, Murat, Kocaman, Selami, Bala, Keziban Asli, Kaba, Sultan, Yel, Servet, Sen, Askin

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The Second and Third Hemoglobin Kansas Cases in the Turkish Population\Türk Popülasyonundaki Ikinci ve Üçüncü Hemoglobin Kansas Olgulari von Tanriverdi, Zeynep Kayra, Akyay, Arzu, Sen, Askin, Taskapan, Çagatay, Özgen, Ünsal

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Pseudohypoparathyroisidm Type 1a: A Case Report von Dogan, Murat, Kocaman, Selami, Bala, Keziban Asli, Kaba, Sultan, Yel, Servet, Sen, Askin

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Two novel mutations in the FRAS1 gene in Fraser Syndrome: Two case reports von Tunç, Senem Yaman, Coskun, Salih, Aagaçayak, Elif, Sen, Askin, Turgut, Abdulkadir, Akin, Gamze, Gül, Talip

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Chromosomal Translocation t (10;19) (q11.2;q13.4) in an Infertile Male/Infertil bir Erkekte t (10;19) (q11.2;q13.4) Kromozomal Translokasyonu von Kara, Murat, Sen, Askin, Cetin, Esin Sakalli, Kargun, Kursat

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Chromosomal Translocation t (10;19) (q11.2;q13.4) in an Infertile Male von Kara, Murat, Sen, Askin, Cetin, Esin Sakallı, Kargun, Kursat

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Effect of Different Shading Practices Used at Pre-harvest Stage on Quality and Storage Life of Sultana Seedless Grapes von Fatih Sen Askin Altun Metin Kesgin Mustafa Sacid Inan

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