A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN
Lehmann, K., Seemann, P., Silan, F., Goecke, T.O., Irgang, S., Kjaer, K.W., Kjaergaard, S., Mahoney, M.J., Morlot, S., Reissner, C., Kerr, B., Wilkie, A.O.M., Mundlos, S.
Published in American journal of human genetics (01.08.2007)
Published in American journal of human genetics (01.08.2007)
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Journal Article
Possible association between germline methylenetetrahydrofolate reductase gene polymorphisms and psoriasis risk in a Turkish population
Kilic, S., Ozdemir, O., Silan, F., Isik, S., Yildiz, O., Karaagacli, D., Silan, C., Ogretmen, Z.
Published in Clinical and experimental dermatology (01.01.2017)
Published in Clinical and experimental dermatology (01.01.2017)
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Journal Article
Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey
Uludağ, A, Uysal, A, Uludağ, A, Ertekin, YH, Tekin, M, Kütük, B, Silan, F, Özdemir, Ö
Published in Balkan journal of medical genetics (01.07.2016)
Published in Balkan journal of medical genetics (01.07.2016)
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Journal Article
The MEFV gene pathogenic variants and phenotype-genotype correlation in children with familial Mediterranean fever in the Çanakkale population
Battal, F, Silan, F, Topaloğlu, N, Aylanç, H, Yıldırım, Ş, Köksal Binnetoğlu, F, Tekin, M, Kaymaz, N, Ozdemir, O
Published in Balkan journal of medical genetics (01.12.2016)
Published in Balkan journal of medical genetics (01.12.2016)
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Journal Article
SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism
Borozdin, W, Boehm, D, Leipoldt, M, Wilhelm, C, Reardon, W, Clayton-Smith, J, Becker, K, Mühlendyck, H, Winter, R, Giray, Ö, Silan, F, Kohlhase, J
Published in Journal of medical genetics (01.09.2004)
Published in Journal of medical genetics (01.09.2004)
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Journal Article
Double translocation: an interesting family history
Uysal, A, Uludağ, A, Sılan, F, Erçelen, N, Zafer, C, Ozdemir, O
Published in Balkan journal of medical genetics (01.06.2013)
Published in Balkan journal of medical genetics (01.06.2013)
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Journal Article
Non‐Hodgkin's lymphoma and auricular hypoplasia: associated with juvenile colloid milium or ligneous conjunctivitis?
Kavak, A, Kaya, M, Alper, M, Çam, M, Büyükbabani, N, Bilen, A, Sılan, F
Published in Journal of the European Academy of Dermatology and Venereology (01.05.2005)
Published in Journal of the European Academy of Dermatology and Venereology (01.05.2005)
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Journal Article
PP-288 Intercellular Adhesion Molecule-1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow
Gazi, E, Barutçu, A, Altun, B, Temiz, A, Bekler, A, Urfalı, M, Sılan, F, Çölkesen, Y, Özdemir, Ö
Published in The American journal of cardiology (01.04.2014)
Published in The American journal of cardiology (01.04.2014)
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Journal Article
Partial trisomy 1(q25qter) due to a de novo unbalanced 1;19 translocation in a neonate
Senses, D A, Silan, F, Uzun, H, Zafer, C, Ucar-Cavusoglu, E, Kocabay, K
Published in Genetic counseling (01.01.2007)
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Published in Genetic counseling (01.01.2007)
Journal Article
Partial trisomy 4(q31qter) due to maternal 4;5 balanced translocation in a neonate
Senses, D A, Silan, F, Uzun, H, Alagöz, D, Zafer, C, Kocabay, K, Karaüzüm, S B, Cetin, Z
Published in Genetic counseling (01.01.2007)
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Published in Genetic counseling (01.01.2007)
Journal Article
Association between FokI , ApaI and TaqI RFLP polymorphisms in VDR gene and H ashimoto's thyroiditis: preliminary data from female patients in S erbia
Djurovic, J., Stojkovic, O., Ozdemir, O., Silan, F., Akurut, C., Todorovic, J., Savic, K., Stamenkovic, G.
Published in International journal of immunogenetics (01.06.2015)
Published in International journal of immunogenetics (01.06.2015)
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Journal Article
Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations
Ozdemir, Oztürk, Yenicesu, Gonca Imir, Silan, Fatma, Köksal, Binnur, Atik, Sinem, Ozen, Filiz, Göl, Mert, Cetin, Ali
Published in Genetic testing and molecular biomarkers (01.04.2012)
Published in Genetic testing and molecular biomarkers (01.04.2012)
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Journal Article
Increased T-allele frequency of 677 C>T polymorphism in the methylenetetrahydrofolate reductase gene in differentiated thyroid carcinoma
Ozdemir, Semra, Silan, Fatma, Hasbek, Zekiye, Uludag, Ahmet, Atik, Sinem, Erselcan, Taner, Ozdemir, Ozturk
Published in Genetic testing and molecular biomarkers (01.07.2012)
Published in Genetic testing and molecular biomarkers (01.07.2012)
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Journal Article
A new mutation of the fukutin gene in a non-Japanese patient
Silan, Fatma, Yoshioka, Mieko, Kobayashi, Kazuhiro, Simsek, Enver, Tunc, Murat, Alper, Murat, Cam, Meryem, Guven, Aysel, Fukuda, Yoji, Kinoshita, Moritoshi, Kocabay, Kenan, Toda, Tatsushi
Published in Annals of neurology (01.03.2003)
Published in Annals of neurology (01.03.2003)
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