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SMOC1 is essential for ocular and limb development in humans and mice.
Okada I, Hamanoue H, Terada K, Tohma T, Megarbane A, Chouery E, Abou-Ghoch J, Jalkh N, Cogulu O, Ozkinay F, Horie K, Takeda J, Furuichi T, Ikegawa S, Nishiyama K, Miyatake S, Nishimura A, Mizuguchi T, Niikawa N, Hirahara F, Kaname T, Yoshiura K, Tsurusaki Y, Doi H, Miyake N, Furukawa T, Matsumoto N, Saitsu H. Okada I, et al. Among authors: cogulu o. Am J Hum Genet. 2011 Jan 7;88(1):30-41. doi: 10.1016/j.ajhg.2010.11.012. Epub 2010 Dec 30. Am J Hum Genet. 2011. PMID: 21194678 Free PMC article.
Does MicroRNA Profile Differ in Early Onset Coronary Artery Disease?
Kahya Eren N, Karaca E, Şirin FB, Levent F, Gündüz C, Özdemir E, Nazlı C, Cogulu O, Ergene AO. Kahya Eren N, et al. Among authors: cogulu o. Turk Kardiyol Dern Ars. 2022 Sep;50(6):407-414. doi: 10.5543/tkda.2022.22408. Turk Kardiyol Dern Ars. 2022. PMID: 36068979 Free article.
Waardenburg anophthalmia syndrome: report and review.
Cogulu O, Ozkinay F, Gündüz C, Sapmaz G, Ozkinay C. Cogulu O, et al. Am J Med Genet. 2000 Jan 17;90(2):173-4. Am J Med Genet. 2000. PMID: 10607960 Review. No abstract available.
Mandibuloacral dysplasia with absent breast development.
Cogulu O, Gunduz C, Arkun R, Darcan S, Kadioglu B, Ozkinay F, Ozkinay C. Cogulu O, et al. Am J Med Genet A. 2003 Jun 15;119A(3):391-2. doi: 10.1002/ajmg.a.10169. Am J Med Genet A. 2003. PMID: 12784312 No abstract available.
Two cases of macrocephaly and immune deficiency.
Cogulu O, Aykut A, Kutukculer N, Ozkinay C, Ozkinay F. Cogulu O, et al. Clin Dysmorphol. 2007 Apr;16(2):81-84. doi: 10.1097/MCD.0b013e3280464ee6. Clin Dysmorphol. 2007. PMID: 17351349
Seckel syndrome with Morgagni hernia.
Onder A, Cogulu O, Ekmekci A, Pariltay E, Kirbiyik O, Ozkinay F. Onder A, et al. Among authors: cogulu o. Clin Dysmorphol. 2007 Jul;16(3):209-210. doi: 10.1097/MCD.0b013e3281c9b08e. Clin Dysmorphol. 2007. PMID: 17551341
163 results