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	1.	Investigation of CYP2D6 Gene Polymorphisms in Turkish Population. [electronic resource] by Taskin, Bayram Percin, Ferda E Ergun, Mehmet Ali Publication details: Psychopharmacology bulletin Mar 2016 In: Psychopharmacology bulletin vol. 46 Availability: No items available. Save to lists Add to cart (remove)
	2.	Evaluation of GenoFlow Thrombophilia Array Test Kit in its detection of mutations in Factor V Leiden (G1691A), prothrombin G20210A, MTHFR C677T and A1298C in blood samples from 113 Turkish female patients. [electronic resource] by Aytekin, Ebru Ergun, Sezen Guntekin Ergun, Mehmet Ali Percin, Ferda E Producer: 20150629 In: Genetic testing and molecular biomarkers vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Lack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish women. [electronic resource] by Percin, Ferda E Cetin, Meral Pinarbasi, Ergun Akgun, Egemen Gurlek, Fatma Cetin, Ali Producer: 20070712 In: European journal of obstetrics, gynecology, and reproductive biology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A Turkish family with Nance-Horan Syndrome due to a novel mutation. [electronic resource] by Tug, Esra Dilek, Nihal F Javadiyan, Shahrbanou Burdon, Kathryn P Percin, Ferda E Producer: 20131113 In: Gene vol. 525 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome. [electronic resource] by Kayhan, Gulsum Ergun, Mehmet Ali Ergun, Sezen Guntekin Kula, Serdar Percin, Ferda E Producer: 20181211 In: Genetic testing and molecular biomarkers vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case. [electronic resource] by Tuğ, Esra Yirmibeş Karaoğuz, Meral Kayhan, Gülsüm Ergün, Mehmet Ali Perçin, Ferda E Producer: 20150818 In: American journal of medical genetics. Part A vol. 164A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Association of microsomal epoxide hydrolase gene polymorphism and pre-eclampsia in Turkish women. [electronic resource] by Pinarbasi, Ergun Percin, Ferda E Yilmaz, Meral Akgun, Egemen Cetin, Meral Cetin, Ali Producer: 20070508 In: The journal of obstetrics and gynaecology research vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	No association of polymorphisms in the glutathione S-transferase genes with pre-eclampsia, eclampsia and HELLP syndrome in a Turkish population. [electronic resource] by Cetin, Meral Pinarbasi, Ergun Percin, Ferda E Akgün, Egemen Percin, Sibel Pinarbasi, Hatice Gurlek, Fatma Cetin, Ali Producer: 20050811 In: The journal of obstetrics and gynaecology research vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Rectal duplications accompanying rectovestibular fistula: report of two cases. [electronic resource] by Pampal, Arzu Ozbayoglu, Asli Kaya, Cem Pehlivan, Yildiz Poyraz, Aylar Ozen, I Onur Percin, Ferda E Demirogullari, Billur Producer: 20140401 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Autosomal recessive mesoaxial synostotic syndactyly with phalangeal reduction maps to chromosome 17p13.3. [electronic resource] by Malik, Sajid Percin, Ferda E Ahmad, Wasim Percin, Sitki Akarsu, Nurten A Koch, Manuela C Grzeschik, Karl-Heinz Producer: 20050627 In: American journal of medical genetics. Part A vol. 134 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Mutations affecting the BHLHA9 DNA-binding domain cause MSSD, mesoaxial synostotic syndactyly with phalangeal reduction, Malik-Percin type. [electronic resource] by Malik, Sajid Percin, Ferda E Bornholdt, Dorothea Albrecht, Beate Percesepe, Antonio Koch, Manuela C Landi, Antonio Fritz, Barbara Khan, Rizwan Mumtaz, Sara Akarsu, Nurten A Grzeschik, Karl-Heinz Producer: 20150227 In: American journal of human genetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)