Showing 1 - 8 results of 8 for search 'Ferda Ozkinay', query time: 0.01s Refine Results
  1. 1
    The second case with 47, XY, + 8 [38] / 45, X0

    The second case with 47, XY, + 8 [38] / 45, X0 by Ozgür Coğulu, Cengiz Tirpan, Ferda Ozkinay, Cumhur Gündüz, Cihangir Ozkinay

    Published 2002-01-01
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  2. 2
    Pyoderma gangrenosum in a six-month-old boy

    Pyoderma gangrenosum in a six-month-old boy by Güldane Koturoğlu, Fadil Vardar, Ferda Ozkinay, Zafer Kurugöl, Taner Akalin, Cihangir Ozkinay

    Published 2006-04-01
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  3. 3
    Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish children

    Mannose-binding lectin gene codon 54 polymorphism susceptible to brucellosis in Turkish children by Nuri Bayram, Ferda Ozkinay, Hüseyin Onay, Dilek Yilmaz-Ciftdoğan, Senem Tufan, Fadil Vardar

    Published 2012-06-01
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  4. 4
    Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene

    Achondroplasia in Turkey is defined by recurrent G380R mutation of the FGFR3 gene by Sacide Pehlivan, Ferda Ozkinay, Ozlem Okutman, Ozgür Coğulu, Ali Ozcan, Tufan Cankaya, Ayfer Ulgenalp

    Published 2003-04-01
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  5. 5
    Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis

    Association between mannose binding lectin polymorphisms and predisposition to bacterial meningitis by Fadil Vardar, Sacide Pehlivan, Hüseyin Onay, Füsun Atlihan, Nesrin Güliz, Cihangir Ozkinay, Ferda Ozkinay

    Published 2007-07-01
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  6. 6
    Mannose-binding lectin may affect pregnancy outcome

    Mannose-binding lectin may affect pregnancy outcome by Şebnem Çalkavur, Fuat Akercan, Ferda Özkınay, Güzide Aksu, Osman Zekioğlu, Mehmet Yalaz, Özge Altun Köroğlu, Hüseyin Onay, Gülin Erdemir, Nilgün Kültürsay

    Published 2015-02-01
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  7. 7
    Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy

    Deletion analysis and clinical correlations in patients with Xp21 linked muscular dystrophy by Ayfer Ulgenalp, Ferda Ozkinay, Eray Dirik, Sarenur Tütüncüoğlu, Gülşen Dizdarer, Nedret Uran, Hatice Karasoy, Gül Sağin-Saylam, Semra Kurul, Tülin Hizli, Elçin Bora, Ozlem Giray, Derya Erçal

    Published 2004-10-01
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  8. 8
    Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.

    Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice. by Joe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, Lisa McKie, Lihadh Al-Gazali, Rosanna Pallotta, Anita Saponari, Peter Branney, Malcolm Fisher, Harris Morrison, Louise Bicknell, Philippe Gautier, Paul Perry, Kishan Sokhi, David Sexton, Tanya M Bardakjian, Adele S Schneider, Nursel Elcioglu, Ferda Ozkinay, Rainer Koenig, Andre Mégarbané, C Nur Semerci, Ayesha Khan, Saemah Zafar, Raoul Hennekam, Sérgio B Sousa, Lina Ramos, Livia Garavelli, Andrea Superti Furga, Anita Wischmeijer, Ian J Jackson, Gabriele Gillessen-Kaesbach, Han G Brunner, Dagmar Wieczorek, Hans van Bokhoven, David R Fitzpatrick

    Published 2011-07-01
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