Changes in the expression and methylation levels of the MMP-2, MMP-9, TIMP-1, TIMP-2 and VEGF-A genes in children with acute lymphoblastic leukemia von İnandıklıoğlu,Nihal, Demirhan,Osman, Bayram,İbrahim, Tanyeli,Atilla

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Can we restore the colour of long‐term discoloured resin composites by noninvasive methods? von Atalayin Ozkaya, Cigdem, Yasa, Bilal, Demirhan, Ali Osman, Turkun, Lezize Sebnem

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Constitutional chromosome 16q mosaicism: Inheritance and phenotypic effects von Demirhan,Osman, Tunç,Erdal, Altınbaşak,Şakir

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Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients von Demirhan, Osman, Tunç, Erdal

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Chromosome aberrations in a schizophrenia population von Demirhan, Osman, Taştemir, Deniz

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Frequency and Types of Chromosomal Abnormalities in Turkish Women with Amenorrhea von Demirhan, Osman, PhD, Tanrıverdi, Nilgün, PhD, Tunç, Erdal, PhD, İnandıklıoğlu, Nihal, PhD, Süleymanova, Dilara, PhD, MD

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Gene Mutations in Chronic Kidney Disease Patients With Secondary Hyperparathyroidism and Sagliker Syndrome von Demirhan, Osman, PhD, Arslan, Ahmet, PhD, Sagliker, Yahya, MD, Akbal, Eylul, PhD, Ergun, Sercan, Bayraktar, Recep, Sagliker, Hasan Sabit, MD, Dogan, Ekrem, MD, Gunesacar, Ramazan, PhD, Ozkaynak, Piril Sagliker, MD

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Cancerous cell lines alter their genomic organization and karyotype with increased passage number: A cytogenetic study von Demirhan,Osman, Pazarbaşı,Ayfer, Özpak,Lütfiye, Tunç,Erdal, Yılmaz,Mehmet Bertan, Ilgaz,N. Seda, Öksüz,Hale, Öztecik,Ezgi

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Identification of the short arm of the Y chromosome by cytogenetic and molecular analyses von Demirhan, Osman, Yilmaz, Mehmet B., Tanriverdi, Nilgun, Kocaturk-Sel, Sabriye, Erkoc, Mehmet A., Oksuz, Hale

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The expression of folate sensitive fragile sites in patients with bipolar disorder von Demirhan, Osman, Tastemir, Deniz, Sertdemir, Yasar

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Report of a New Case With Pentasomy X and Novel Clinical Findings von Demirhan, Osman, Tanriverdi, N, Yilmaz, M.B, Kocaturk-Sel, S, Inandiklioglu, N, Luleyap, U, Akbal, E, Comertpay, G, Tufan, T, Dur, O

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Chromosomal fragile site expression in Turkish psychiatric patients von Taştemir, Deniz, Demirhan, Osman, Sertdemir, Yaşar

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International Evaluation of Unrecognizably Uglifying Human Faces in Late and Severe Secondary Hyperparathyroidism in Chronic Kidney Disease. Sagliker Syndrome. A Unique Catastrophi... von Yildiz, Ismail, MD, Sagliker, Yahya, MD, Demirhan, Osman, MD, Tunc, Erdal, PhD, Inandiklioglu, Nihal, PhD, Tasdemir, Deniz, PhD, Acharya, Vidya, MD, Zhang, Ling, MD, Golea, Ovidia, MD, Sabry, Alaa, MD, Ookalkar, Dhananjay S., MD, Capusa, Cristina, MD, Radulescu, Dana, MD, Garneata, Liliana, MD, Mircescu, Gabriel, MD, Ben Maiz, Hedi, MD, Hsu Chen, Cheng, MD, Prado Rome, Jorge, MD, Benzegoutta, Mansour, MD, Paylar, Nuray, PhD, Eyuboglu, Kamil, MD, Karatepe, Ersin, MD, Esenturk, Mustafa, MD, Yavascan, Onder, MD, Grzegorzevska, Alicza, MD, Shilo, Valery, MD, Mazdeh, Mitra Mahdavi, MD, Francesco, Ramos Carillo, MD, Gouda, Zaghloul, MD, Adam, Siddik Momin, MD, Emir, Idris, MD, Ocal, Faith, MD, Usta, Erol, MD, Kiralp, Necati, MD, Sagliker, Cemal, MD, Ozkaynak, Piril Sagliker, MD, Sagliker, Hasan Sabit, MD, Bassuoni, Mahmoud, MD, Sekin, Oktay, MD

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Modifications of the locomotor system in habitually quadrupedal humans von Tardieu, Christine, Demirhan, Osman, Akbal, Eylül, Ozgozen, Levent, Biçer, Ömer Sunkar, Delapré, Arnaud, Cornette, Raphaël, Herrel, Anthony

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P0907STRIKING NOVEL MULTI-MISMUTATIONS ON GNAS1,FGF23,FGFR3 GENES IN CKD WITH SECONDARY HYPERPARATHYROIDISM.(SH).SAGLIKER SYNDROME(SS).SS IS A COMBINATION-COMPULSION OF BONE DYSPLA... von Sagliker, Yahya, Demirhan, Osman, Sagliker, Hasan Sabit, Sagliker Ozkaynak, Piril, Paylar, Nuray, Sagliker, Cemal, Emir, Idris, Ozkaynak, Isıl

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Chromosomal analyses of 1510 couples who have experienced recurrent spontaneous abortions von Tunç, Erdal, Tanrıverdi, Nilgün, Demirhan, Osman, Süleymanova, Dilara, Çetinel, Nesrin

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Are there fetal stem cells in the maternal brain von Demirhan, Osman, Cekin, Necmi, Taştemir, Deniz, Tunç, Erdal, Güzel, Ali İrfan, Meral, Demet, Demirbek, Bülent

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Effect Of Conception Time And Maternal Age Upon Fetal Sex Ratio In Çukurova Population von Kasap,Mülkiye, Güzel,Ali İrfan, Demirhan,Osman, Pazarbaşı,Ayfer, Özgünen,Fatma Tuncay, Tunç,Erdal, Taştemir Korkmaz,Deniz, Yılmaz,Bertan, Kocatürk Sel,Sabriye

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Inheritance of pericentric inversion in chromosome 7 through the three progenies and a newborn with congenital hydronephrosis diagnosed prenatally by fetal urine sampling von Demirhan, Osman, Ph.D, Özcan, Kenan, M.D, Taştemir, Deniz, M.Sc, Demir, Cansun, M.D, Tunç, Erdal, M.Sc, Solğun, Hüseyin A., M.D, Güzel, Ali İrfan, Ph.D

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Interrelation of aromatase, estrogen receptor alpha and progesterone receptor in the developing mouse fetal brain von Mehmet Bertan Yilmaz, Mehmet Ali Erkoc, Sabriye Kocaturk-Sel, Erdal Tunc, Lutfiye Ozpak, Ayfer Pazarbasi, Ali Irfan Guzel, Davut Alptekin, Husnu Umit Luleyap, Osman Demirhan, Mulkiye Kasap, Halil Kasap

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