A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies
Demirhan, O, Türkmen, S, Schwabe, G C, Soyupak, S, Akgül, E, Taştemir, D, Karahan, D, Mundlos, S, Lehmann, K
Published in Journal of medical genetics (01.04.2005)
Published in Journal of medical genetics (01.04.2005)
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Journal Article
Inheritance of a translocation between chromosomes 12 and 16 in a family with recurrent miscarriages and a newborn with Down syndrome carrying the same translocation
Pazarbaşi, A, Demirhan, O, Turgut, M, Güzel, I, Taştemir, D
Published in Genetic counseling (01.01.2008)
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Published in Genetic counseling (01.01.2008)
Journal Article
Prenatal Diagnosis of Translocation 13;13 Patau Syndrome: Clinical Features of Two Cases
Pazarbaşi, A, Demirhan, O, Süleymanova-Karahan, D, Taştemir, D, Tunç, E, Gümürdülü, D
Published in Balkan journal of medical genetics (01.01.2008)
Published in Balkan journal of medical genetics (01.01.2008)
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Journal Article
Cytogenetic study of recurrent miscarriages and their parents
Tunç, E., Demirhan, O., Demir, C., Taştemir, D.
Published in Russian journal of genetics (01.04.2007)
Published in Russian journal of genetics (01.04.2007)
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Journal Article
The protective effect of resveratrol against risperidone-induced liver damage through an action on FAS gene expression
Azirak, Sebile, Bilgic, Sedat, Tastemir Korkmaz, Deniz, Guvenc, Ayşe N, Kocaman, Nevin, Ozer, Mehmet K
Published in General physiology and biophysics (01.01.2019)
Published in General physiology and biophysics (01.01.2019)
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Journal Article
The reliability of maternal serum triple test in prenatal diagnosis of fetal chromosomal abnormalities of pregnant Turkish women
Demirhan, Osman, Pazarbaşı, Ayfer, Güzel, Ali İrfan, Taştemir, Deniz, Yilmaz, Bertan, Kasap, Mülkiye, Özgünen, Fatma Tuncay, Evrüke, Cüneyt, Demir, Cansun, Tunç, Erdal, Kocatürk-Sel, Sabriye, Onatoğlu-Arikan, Dilge, Koç, Semra, Özer, Onur, İnandiklioğlu, Nihal
Published in Genetic testing and molecular biomarkers (01.10.2011)
Published in Genetic testing and molecular biomarkers (01.10.2011)
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Journal Article
Detection of parental origin and cell stage errors of a double nondisjunction in a fetus by QF-PCR
Guzel, Ali Irfan, Demirhan, Osman, Pazarbasi, Ayfer, Ozgunen, Fatma Tuncay, Kocaturk-Sel, Sabriye, Tastemir, Deniz
Published in Genetic testing and molecular biomarkers (01.02.2009)
Published in Genetic testing and molecular biomarkers (01.02.2009)
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Journal Article
The first report described as an important study: The association of mannose-binding lectin gene 2 polymorphisms in children with Down syndrome
Demirhan, Osman, Taştemir, Deniz, Güneşaçar, Ramazan, Güzel, Ali İrfan, Alptekin, Davut
Published in Indian journal of human genetics (01.05.2011)
Published in Indian journal of human genetics (01.05.2011)
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