Simşek PO - Search Results

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Rare sex chromosome aneuploidies: 49,XXXXY and 48,XXXY syndromes.

Simşek PO, Utine GE, Alikaşifoğlu A, Alanay Y, Boduroğlu K, Kandemir N. Simşek PO, et al. Turk J Pediatr. 2009 May-Jun;51(3):294-7. Turk J Pediatr. 2009. PMID: 19817277

PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents.

Çelik T, Simsek PO, Sozen T, Ozyuncu O, Utine GE, Talim B, Yiğit Ş, Boduroglu K, Kamnasaran D. Çelik T, et al. Among authors: simsek po. Clin Genet. 2012 Mar;81(3):294-7. doi: 10.1111/j.1399-0004.2011.01730.x. Epub 2011 Dec 28. Clin Genet. 2012. PMID: 22211708 No abstract available.

A case of congenital agenesis of the right pulmonary artery presenting with hemoptysis and mimicking pulmonary hemosiderosis.

Simsek PO, Ozcelik U, Celiker A, Yalcin E, Cobanoglu N, Pekcan S, Alehan D, Ucar C, Dogru D, Kiper N. Simsek PO, et al. Eur J Pediatr. 2009 Feb;168(2):217-20. doi: 10.1007/s00431-008-0726-x. Epub 2008 May 14. Eur J Pediatr. 2009. PMID: 18478262

Tracheobronchopathia osteochondroplastica in a 9-year-old girl.

Simsek PO, Ozcelik U, Demirkazik F, Unal OF, Orhan D, Aslan AT, Dogru D. Simsek PO, et al. Pediatr Pulmonol. 2006 Jan;41(1):95-7. doi: 10.1002/ppul.20311. Pediatr Pulmonol. 2006. PMID: 16284968

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