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	1.	Treatment of three hereditary leiomyomatosis patients with cryotherapy. [electronic resource] by Uyar, Belkız Acar, Emine M Subaşıoğlu, Aslı Producer: 20210514 In: Dermatologic therapy vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Genetic background of supernumerary teeth. [electronic resource] by Subasioglu, Aslı Savas, Selcuk Kucukyilmaz, Ebru Kesim, Servet Yagci, Ahmet Dundar, Munis Producer: 20150225 In: European journal of dentistry vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The effect of the additional cytogenetic abnormalities on major molecular response and BCR-ABL kinase domain mutations in long-term follow-up chronic myeloid leukemia patients, a cross sectional study. [electronic resource] by Savasoglu, Kaan Payzin, Kadriye Bahriye Ozdemirkiran, Fusun Subasioglu, Asli Yilmaz, Asu Fergun Producer: 20180112 In: Leukemia & lymphoma vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The effect of parental 5,10-methylenetetrahydrofolate reductase 677C/T and 1298A/C gene polymorphisms on response to single-dose methotrexate in tubal ectopic pregnancy. [electronic resource] by Kutuk, Mehmet Serdar Subasioglu, Asli Uludag, Semih Tascioglu, Nazife Ozgun, Mahmut Tuncay Dundar, Munis Producer: 20180222 In: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Emopamil binding protein mutation in conradi-hünermann-happle syndrome representing plaque-type psoriasis. [electronic resource] by Ozyurt, Kemal Subasioglu, Asli Ozturk, Perihan Inci, Rahime Ozkan, Fuat Bueno, Elena Cañueto, Javier González Sarmiento, Rogelio Producer: 20150327 In: Indian journal of dermatology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A Glutamine Repeat Variant of the RUNX2 Gene Causes Cleidocranial Dysplasia. [electronic resource] by Mastushita, Masaki Kitoh, Hiroshi Subasioglu, Asli Kurt Colak, Fatma Dundar, Munis Mishima, Kenichi Nishida, Yoshihiro Ishiguro, Naoki Producer: 20150408 In: Molecular syndromology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Research of genetic bases of hereditary non-syndromic hearing loss. [electronic resource] by Subaşıoğlu, Aslı Duman, Duygu Sırmacı, Aslı Bademci, Güney Carkıt, Fehime Somdaş, Mehmet Akif Erkan, Mustafa Tekin, Mustafa Dündar, Munis Publication details: Turk pediatri arsivi Sep 2017 In: Turk pediatri arsivi vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Novel domain-specific POU3F4 mutations are associated with X-linked deafness: examples from different populations. [electronic resource] by Bademci, Guney Lasisi, Akeem Yariz, Kemal O Montenegro, Paola Menendez, Ibis Vinueza, Rodrigo Paredes, Rosario Moreta, Germania Subasioglu, Asli Blanton, Susan Fitoz, Suat Incesulu, Armagan Sennaroglu, Levent Tekin, Mustafa Producer: 20150630 In: BMC medical genetics vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Dysfunction of [electronic resource] by Li, Chong Bademci, Guney Subasioglu, Asli Diaz-Horta, Oscar Zhu, Yi Liu, Jiaqi Mitchell, Timothy Gavin Abad, Clemer Seyhan, Serhat Duman, Duygu Cengiz, Filiz Basak Tokgoz-Yilmaz, Suna Blanton, Susan H Farooq, Amjad Walz, Katherina Zhai, R Grace Tekin, Mustafa Producer: 20190325 In: Proceedings of the National Academy of Sciences of the United States of America vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. [electronic resource] by Bademci, Guney Foster, Joseph Mahdieh, Nejat Bonyadi, Mortaza Duman, Duygu Cengiz, F Basak Menendez, Ibis Diaz-Horta, Oscar Shirkavand, Atefeh Zeinali, Sirous Subasioglu, Asli Tokgoz-Yilmaz, Suna Huesca-Hernandez, Fabiola de la Luz Arenas-Sordo, Maria Dominguez-Aburto, Juan Hernandez-Zamora, Edgar Montenegro, Paola Paredes, Rosario Moreta, Germania Vinueza, Rodrigo Villegas, Franklin Mendoza-Benitez, Santiago Guo, Shengru Bozan, Nazim Tos, Tulay Incesulu, Armagan Sennaroglu, Gonca Blanton, Susan H Ozturkmen-Akay, Hatice Yildirim-Baylan, Muzeyyen Tekin, Mustafa Producer: 20161219 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)