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A Null Mutation of TNFRSF11A Causes Dysosteosclerosis, Not Osteopetrosis.
Kırkgöz T, Özkan B, Hazan F, Acar S, Nalbantoğlu Ö, Özkaya B, Kulalı MA, Gürsoy S, Ikegawa S, Guo L. Kırkgöz T, et al. Among authors: hazan f. Front Genet. 2022 Jun 24;13:938814. doi: 10.3389/fgene.2022.938814. eCollection 2022. Front Genet. 2022. PMID: 35812760 Free PMC article.
Association of Wolfram syndrome with Fallot tetralogy in a girl.
Korkmaz HA, Demir K, Hazan F, Yıldız M, Elmas ÖN, Özkan B. Korkmaz HA, et al. Among authors: hazan f. Arch Argent Pediatr. 2016 Jun 1;114(3):e163-6. doi: 10.5546/aap.2016.eng.e163. Epub 2016 Jun 1. Arch Argent Pediatr. 2016. PMID: 27164349 Free article. English, Spanish.
The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome.
Gürsoy S, Kutbay YB, Özdemir TR, Hazan F. Gürsoy S, et al. Among authors: hazan f. Turk J Pediatr. 2019;61(4):589-593. doi: 10.24953/turkjped.2019.04.017. Turk J Pediatr. 2019. PMID: 31990478 Free article.
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic disorder: 2q37 deletion syndrome. ...
Gursoy S, Kutbay YB, Ozdemir TR, Hazan F. The clinical and molecular features of three Turkish patients with a rare genetic di …
58 results