Orodental, Facial and Clinical Features of Mutation-Positive Noonan Syndrome: A Monocentric Study von Gürsoy, Semra, Hazan, Filiz, Kaderli, Bülent, Meşe, Timur, Tükün, Ajlan

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Evaluation of clinical findings and neurofibromatosis type 1 bright objects on brain magnetic resonance images of 60 Turkish patients with NF1 gene variants von Hazan, Filiz, Gürsoy, Semra, Unalp, Aycan, Yılmaz, Unsal, Demirağ, Bengü, Aydin Köker, Sultan, Ozyılmaz, Berk, Erdogan, Kadri Murat, Kalenderer, Önder, Erkuş, Serkan, Gürçınar, Müge, Tükün, Ajlan

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Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment von Kaymak Cihan, Meriç, Karabulut, Halil Gürhan, Yürür Kutlay, Nüket, Ilgın Ruhi, Hatice, Tükün, Ajlan, Olcay, Lale

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Expression of Survivin and Its Splice Variants in Pediatric Acute Lymphoblastic Leukemia von Eren-Keleş, Efsun, Karabulut, Halil Gürhan, Çakmaklı, Hasan Fatih, Adaklı, Başak, Köse, Serdar Kenan, Uğur-Dinçaslan, Handan, Yavuz, Gülsan, Ertem, Mehmet, Tükün, Ajlan

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Molecular Testing for Thalassemia: Mutation Detection According to Referral Reasons and Demographic Data von Altıner, Şule, Karabulut, Halil Gürhan, Ekinci, Sadiye, Vicdan, Arzu, Kutlay, Nüket, Tuncalı, Timur, Ajlan Tükün, Ruhi, Hatice Ilgın

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Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion von Çelik, Vesile Deniz, Kiliç, Betul Orhan, Akişin, Yasemin Ardiçoğlu, Tükün, Fatma Ajlan, Akar, Nejat

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The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does “disorders of sexual development (DSD)” classification based on new Chicago consensus cover all sex chromos... von Öcal, Gönül, Berberoğlu, Merih, Şıklar, Zeynep, Ruhi, Hatice Ilgın, Tükün, Ajlan, Çamtosun, Emine, Erdeve, Şenay Savaş, Hacıhamdioğlu, Bülent, Fitöz, Suat

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The association between telomere length and ischemic stroke risk and phenotype von Yetim, Ezgi, Topcuoglu, Mehmet Akif, Yurur Kutlay, Nuket, Tukun, Ajlan, Oguz, Kader K., Arsava, Ethem Murat

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Is telomere length one of the determinants of reproductive life span? von Aydos, Sena E, Elhan, Atilla H, Tükün, Ajlan

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Genetic Approach to Thyroid Nodules and Cancer von Tükün, Ajlan

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Biology of Stem Cells in Human Umbilical Cord Stroma: In Situ and In Vitro Surveys von Karahuseyinoglu, Sercin, Cinar, Ozgur, Kilic, Emine, Kara, Fadil, Akay, Guvem Gumus, Demiralp, Duygu Özel, Tukun, Ajlan, Uckan, Duygu, Can, Alp

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Psychometric liability to psychosis and childhood adversities are associated with shorter telomere length: A study on schizophrenia patients, unaffected siblings, and non-clinical... von Çevik, Burcu, Mançe-Çalışır, Öykü, Atbaşoğlu, Eşref Cem, Saka, Meram Can, Alptekin, Köksal, Üçok, Alp, Sırmatel, Burcu, Gülöksüz, Sinan, Tükün, Ajlan, van Os, Jim, Gümüş-Akay, Güvem

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Melanocortin-4 Receptor Gene Mutations in a Group of Turkish Obese Children and Adolescents von Tunç, Selma, Demir, Korcan, Tükün, Fatma Ajlan, Topal, Cihan, Hazan, Filiz, Sağlam, Burcu, Nalbantoğlu, Özlem, Yıldız, Melek, Özkan, Behzat

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Vitamin D receptor polymorphisms and bone health after kidney transplantation von KORUCU, Berfu, TÜKÜN, Ajlan, HELVACI, Özant, YETER, Hasan, GÖNEN, Sevim, GÜZ, Galip, ARINSOY, Turgay

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A rare cause of hydrops fetalis in two Gaucher disease type 2 patients with a novel mutation von Kılavuz, Sebile, Basaranoglu, Murat, Epcacan, Serdar, Bako, Derya, Ozer, Arife, Donmez, Yasemin Nuran, Ceylan, Emine Ipek, Tukun, Ajlan, Ceylaner, Serdar, Geylani, Hadi, Mungan, Halise Neslihan Onenli

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Histopathological and genetic features of patients with limb girdle muscular dystrophy type 2C von Dınız, Gülden, Hazan, Filiz, Yildirim, Hülya Tosun, Unalp, Aycan, Polat, Muzaffer, Serdaroğlu, Gül, Güzel, Orkide, Bağ, Ozlem, Seçıl, Yaprak, Ozgönül, Figen, Türe, Sabiha, Akhan, Galip, Tükün, Ajlan

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Association Between N363S and Bcl/Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment von Cihan, Meriç Kaymak, Karabulut, Halil Gürhan, Kutlay, Nüket Yürür, Ruhi, Hatice Ilgın, Tükün, Ajlan, Olcay, Lale

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Unusual Chromosomal Rearrangement Resulted in Interstitial Monosomy 9p: Case Report von Durmaz, Ceren D., Yararbaş, Kanay, Kutlay, Nüket Y., Türedi, Özlem, Akın, İsmigül, Gürbüz, Cansu, Karataş, Günay, Tükün, Ajlan

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Trichorhinophalangeal syndrome type II presenting with short stature in a child von Hazan, Filiz, Korkmaz, Hüseyin A, Yararbaş, Kanay, Wuyts, Wim, Tükün, Ajlan

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Two acute myeloblastic leukemia cases concomitant with hemophagocytic lymphohistiocytosis and review of the literature von Akyay, Arzu, Celkan, Tiraje, Iskender, Gülşen, Tükün, Ajlan, Ogan, Cihat, Olcay, Lale

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