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87 results
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Tigroid pattern on magnetic resonance imaging in Lowe syndrome.
Onur MR, Senol U, Mihçi E, Lüleci E. Onur MR, et al. Among authors: mihci e. J Clin Neurosci. 2009 Jan;16(1):112-4. doi: 10.1016/j.jocn.2008.02.011. Epub 2008 Nov 20. J Clin Neurosci. 2009. PMID: 19022672
Comprehensive dental management in a Hallermann-Streiff syndrome patient with unusual radiographic appearance of teeth.
Gungor OE, Nur BG, Yalcin H, Karayilmaz H, Mihci E. Gungor OE, et al. Among authors: mihci e. Niger J Clin Pract. 2015 Jul-Aug;18(4):559-62. doi: 10.4103/1119-3077.156910. Niger J Clin Pract. 2015. PMID: 25966733
Evaluation of a fetus with Neu-Laxova syndrome through prenatal, clinical, and pathological findings.
Mihci E, Simsek M, Mendilcioglu I, Tacoy S, Karaveli S. Mihci E, et al. Fetal Diagn Ther. 2005 May-Jun;20(3):167-70. doi: 10.1159/000083898. Fetal Diagn Ther. 2005. PMID: 15824491
Possible autosomal recessive inheritance in an infant with acrofacial dysostosis similar to Nager syndrome.
Nur BG, Bernier FP, Oztekin O, Kardelen F, Kalay S, Parboosingh JS, Mihci E. Nur BG, et al. Among authors: mihci e. Am J Med Genet A. 2013 Sep;161A(9):2311-5. doi: 10.1002/ajmg.a.36051. Epub 2013 Aug 2. Am J Med Genet A. 2013. PMID: 23913624
Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene.
Güzel Nur B, Çelmeli G, Manguoğlu E, Soyucen E, Bircan İ, Mıhçı E. Güzel Nur B, et al. Among authors: mihci e. J Clin Res Pediatr Endocrinol. 2016 Sep 1;8(3):360-4. doi: 10.4274/jcrpe.2798. Epub 2016 Apr 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 27086862 Free PMC article.
Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome.
Yakut S, Mihci E, Altiok Clark O, Cetin Z, Keser I, Berker S, Luleci G. Yakut S, et al. Among authors: mihci e. Balkan J Med Genet. 2012 Jun;15(1):61-4. doi: 10.2478/v10034-012-0010-2. Balkan J Med Genet. 2012. PMID: 24052725 Free PMC article.
Unilateral pulmonary agenesis associated with colloidal goiter in a newborn: a case report.
Gökhan GA, Ozbilim G, Bozova S, Güra A, Ongun H, Mihci E, Arslan G. Gökhan GA, et al. Among authors: mihci e. Turk J Pediatr. 2005 Jul-Sep;47(3):295-7. Turk J Pediatr. 2005. PMID: 16250321
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.
Acuna-Hidalgo R, Deriziotis P, Steehouwer M, Gilissen C, Graham SA, van Dam S, Hoover-Fong J, Telegrafi AB, Destree A, Smigiel R, Lambie LA, Kayserili H, Altunoglu U, Lapi E, Uzielli ML, Aracena M, Nur BG, Mihci E, Moreira LM, Borges Ferreira V, Horovitz DD, da Rocha KM, Jezela-Stanek A, Brooks AS, Reutter H, Cohen JS, Fatemi A, Smitka M, Grebe TA, Di Donato N, Deshpande C, Vandersteen A, Marques Lourenço C, Dufke A, Rossier E, Andre G, Baumer A, Spencer C, McGaughran J, Franke L, Veltman JA, De Vries BB, Schinzel A, Fisher SE, Hoischen A, van Bon BW. Acuna-Hidalgo R, et al. Among authors: mihci e. PLoS Genet. 2017 Mar 27;13(3):e1006683. doi: 10.1371/journal.pgen.1006683. eCollection 2017 Mar. PLoS Genet. 2017. PMID: 28346496 Free PMC article.
Prenatal diagnosis of mobile flap-like tissue on the ventricular septal defect in a newborn with trisomy 18.
Kocabas A, Akcan AB, Kardelen F, Mendilcioğlu I, Mıhcı E, Akçurin G, Ertuğ H, Oygür N. Kocabas A, et al. Among authors: mihci e. Echocardiography. 2011 Oct;28(9):E191-3. doi: 10.1111/j.1540-8175.2011.01502.x. Epub 2011 Sep 19. Echocardiography. 2011. PMID: 21933268
Aplasia cutis congenita: three cases with three different underlying etiologies.
Mihçi E, Erişir S, Taçoy S, Lüleci G, Alpsoy E, Oygür N. Mihçi E, et al. Turk J Pediatr. 2009 Sep-Oct;51(5):510-4. Turk J Pediatr. 2009. PMID: 20112612
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