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	1.	Detection of CFTR mutations using temporal temperature gradient gel electrophoresis. [electronic resource] by Wong, Lee-Jun C Alper, Ozgül M Producer: 20050119 In: Electrophoresis vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel human pathological mutations. Gene symbol: TPO. Disease: Thyroid peroxidase deficiency. [electronic resource] by Alper, Ozgul Turkkahraman, Doga Bircan, Iffet Luleci, Guven Producer: 20100217 In: Human genetics vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	3.	Coronal craniosynostosis due to TCF12 mutations in patients from Turkey. [electronic resource] by Yilmaz, Elanur Mihci, Ercan Nur, Banu Alper, Ozgul M Producer: 20200804 In: American journal of medical genetics. Part A vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A novel AXIN2 gene mutation in sagittal synostosis. [electronic resource] by Yilmaz, Elanur Mihci, Ercan Guzel Nur, Banu Alper, Ozgul M Producer: 20190911 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Recent Advances in Craniosynostosis. [electronic resource] by Yilmaz, Elanur Mihci, Ercan Nur, Banu Alper, Özgül M Taçoy, Şükran Producer: 20200729 In: Pediatric neurology vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Normal sweat chloride test does not rule out cystic fibrosis. [electronic resource] by Başaran, Abdurrahman Erdem Karataş-Torun, Nimet Maslak, İbrahim Cemal Bingöl, Ayşen Alper, Özgül M Producer: 20171204 In: The Turkish journal of pediatrics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Mitochondrial ATPase subunit 6 and cytochrome B gene variations in obese Turkish children. [electronic resource] by Demir, Durkadın Türkkahraman, Doğa Aktaş Samur, Anıl Lüleci, Güven Akçurin, Sema Alper, Özgül M Producer: 20160111 In: Journal of clinical research in pediatric endocrinology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Clinical and genetic findings of two cases with Apert syndrome. [electronic resource] by Cammarata-Scalisi, Francisco Yilmaz, Elanur Callea, Michele Avendaño, Andrea Mıhçı, Ercan Alper, Ozgul M Producer: 20200130 In: Boletin medico del Hospital Infantil de Mexico vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	The necessity of complete CFTR mutational analysis of an infertile couple before in vitro fertilization. [electronic resource] by Wong, Lee-Jun C Alper, Ozgül M Hsu, Evelyn Woo, Marlyn S Margetis, Monique F Producer: 20041123 In: Fertility and sterility vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Two novel null mutations in a Taiwanese cystic fibrosis patient and a survey of East Asian CFTR mutations. [electronic resource] by Wong, Lee-Jun C Alper, Ozgül M Wang, Bao-Tyan Lee, Mei-Hui Lo, Shin-Yu Producer: 20040220 In: American journal of medical genetics. Part A vol. 120A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A cystic fibrosis patient with two novel mutations in mitochondrial DNA: mild disease led to delayed diagnosis of both disorders. [electronic resource] by Wong, Lee-Jun C Liang, Min-Hui Kwon, Haeyoung Bai, Ren-Kui Alper, Ozgül Gropman, Andrea Producer: 20030326 In: American journal of medical genetics vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Final diagnosis in children with subclinical hypothyroidism and mutation analysis of the thyroid peroxidase gene (TPO). [electronic resource] by Turkkahraman, Doga Alper, Ozgul M Aydin, Funda Yildiz, Akin Pehlivanoglu, Suray Luleci, Guven Akcurin, Sema Bircan, Iffet Producer: 20100105 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Analysis of TPO gene in Turkish children with iodide organification defect: identification of a novel mutation. [electronic resource] by Turkkahraman, Doga Alper, Ozgul M Pehlivanoglu, Suray Aydin, Funda Yildiz, Akin Luleci, Guven Akcurin, Sema Bircan, Iffet Producer: 20110303 In: Endocrine vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	First prenatal exclusion of cystic fibrosis in East Asia. [electronic resource] by Wong, Lee-Jun C Lee, Mei-Hui Chen, Ming Alper, Ozgül M Tsao, Long-Yen Wang, Bao-Tyan Producer: 20080201 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review. [electronic resource] by Nur, Banu G Pehlivanoğlu, Suray Mıhçı, Ercan Calışkan, Mualla Demir, Durkadın Alper, Ozgül M Kayserili, Hülya Lüleci, Güven Producer: 20141204 In: Pediatric neurology vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	1154insTC is not a rare CFTR mutation. [electronic resource] by Alper, Ozgül M Wong, Lee-Jun C Hostetter, Galen Cook, James Tenenholz, Beverly Hsu, Evelyn Woo, Marlyn S Producer: 20040220 In: American journal of medical genetics. Part A vol. 120A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens. [electronic resource] by Wu, Chien-Chih Alper, Ozgül M Lu, Jyh-Feng Wang, Song-Ping Guo, Li Chiang, Han-Sun Wong, Lee-Jun C Producer: 20051020 In: Human reproduction (Oxford, England) vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Detection of novel CFTR mutations in Taiwanese cystic fibrosis patients. [electronic resource] by Alper, Ozgül M Shu, San-Ging Lee, Mei-Hui Wang, Bao-Tyan Lo, Shin-Yu Lin, Keh-Liang Chiu, Ya-Lan Wong, Lee-Jun C Producer: 20031002 In: Journal of the Formosan Medical Association = Taiwan yi zhi vol. 102 Availability: No items available. Save to lists Add to cart (remove)
	19.	Assessment of women who applied for the uterine transplant project as potential candidates for uterus transplantation. [electronic resource] by Erman Akar, Munire Ozekinci, Murat Alper, Ozgul Demir, Durkadin Cevikol, Can Meric Bilekdemir, Asli Daloglu, Aylin Ongut, Gozde Senol, Yesim Ozdem, Sebahat Uzun, Gulbahar Luleci, Guven Suleymanlar, Gultekin Producer: 20161017 In: The journal of obstetrics and gynaecology research vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia. [electronic resource] by Demir Eksi, Durkadin Shen, Yiping Erman, Munire Chorich, Lynn P Sullivan, Megan E Bilekdemir, Meric Yılmaz, Elanur Luleci, Guven Kim, Hyung-Goo Alper, Ozgul M Layman, Lawrence C Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 26 results.