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	1.	A Baseline Algorithm for Molecular Diagnosis of Genetic Eye Diseases: Ophthalmologist's Perspective. [electronic resource] by Taylan Şekeroğlu, Hande Utine, Gülen Eda Alikaşifoğlu, Mehmet Publication details: Turkish journal of ophthalmology Dec 2016 In: Turkish journal of ophthalmology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	CYP1A1 polymorphism in adolescents with polycystic ovary syndrome. [electronic resource] by Akgül, Sinem Derman, Orhan Alikaşifoğlu, Mehmet Aktaş, Dilek Producer: 20110406 In: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Serum alpha-fetoprotein level in Fanconi's anemia: evaluation of 33 Turkish patients. [electronic resource] by Aslan, Deniz Gümrük, Fatma Alikaşifoğlu, Mehmet Altay, Ciğdem Producer: 20021231 In: American journal of hematology vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience. [electronic resource] by Ardıçlı, Didem Haliloğlu, Goknur Alikaşifoğlu, Mehmet Topaloğlu, Haluk Producer: 20191230 In: Neuropediatrics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Two siblings with similar phenotypes: one of them had ring 20 chromosome. [electronic resource] by Tezer, F Irsel Aktas, Dilek Alikasifoglu, Mehmet Saygi, Serap Producer: 20130709 In: Clinical EEG and neuroscience vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy. [electronic resource] by Sonmez, Fatma Mujgan Uctepe, Eyyup Aktas, Dilek Alikasifoglu, Mehmet Publication details: Intractable & rare diseases research Feb 2017 In: Intractable & rare diseases research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Genetic Variations in Attention Deficit Hyperactivity Disorder Subtypes and Treatment Resistant Cases. [electronic resource] by Unal, Dilek Unal, Mehmet Fatih Alikasifoglu, Mehmet Cetinkaya, Arda Producer: 20160802 In: Psychiatry investigation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Central precocious puberty in a girl with Williams syndrome: the result of treatment with GnRH analogue. [electronic resource] by Utine, G Eda Alikasifoglu, Ayfer Alikasifoglu, Mehmet Tuncbilek, Ergul Producer: 20060426 In: European journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Five Fanconi anemia patients with unusual organ pathologies. [electronic resource] by Unal, Selma Ozbek, Namik Kara, Abdurrahman Alikaşifoĝlu, Mehmet Gümrük, Fatma Producer: 20040921 In: American journal of hematology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Analysis of MTHFR 1298A>C in addition to MTHFR 677C>T polymorphism as a risk factor for neural tube defects in the Turkish population. [electronic resource] by Boduroğlu, Koray Alanay, Yasemin Alikaşifoğlu, Mehmet Aktaş, Dilek Tunçbilek, Ergül Producer: 20060110 In: The Turkish journal of pediatrics vol. 47 Availability: No items available. Save to lists Add to cart (remove)
	11.	Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis. [electronic resource] by Aktas, Dilek Alikasifoglu, Mehmet Gonc, Nazli Senocak, Mehmet E Tuncbilek, Ergul Producer: 20090416 In: European journal of medical genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel missense mutation of the GRK1 gene in Oguchi disease. [electronic resource] by Teke, Mehmet Yasin Citirik, Mehmet Kabacam, Serkan Demircan, Suleyman Alikasifoglu, Mehmet Producer: 20170406 In: Molecular medicine reports vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Factor V Leiden mutation and type 1 diabetes mellitus. [electronic resource] by Demirer, Asli Nar Alikasifoglu, Mehmet Tuncbilek, Ergul Karakus, Sema Erbas, Tomris Producer: 20080331 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Partial distal aphalangia, duplication of metatarsal IV, microcephaly and borderline intelligence: a third patient suggesting autosomal recessive inheritance. [electronic resource] by Utine, Gülen Eda Alanay, Yasemin Aktaş, Dilek Alikaşifoğlu, Mehmet Boduroğlu, Koray Producer: 20090730 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Association of assisted reproductive technology with twinning and congenital anomalies. [electronic resource] by Balci, Sevim Engiz, Ozlem Alikasifoglu, Mehmet Esinler, Ibrahim Sinan Beksac, M Producer: 20081201 In: Indian journal of pediatrics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Methylene tetrahydrofolate reductase polymorphisms and homocysteine level in heart defects. [electronic resource] by Sahiner, Umit M Alanay, Yasemin Alehan, Dursun Tuncbilek, Ergul Alikasifoglu, Mehmet Producer: 20150710 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	CYP1A1 gene polymorphism and risk of epithelial ovarian neoplasm. [electronic resource] by Aktas, Dilek Guney, Inci Alikasifoglu, Mehmet Yüce, Kunter Tuncbilek, Ergul Ayhan, Ali Producer: 20020822 In: Gynecologic oncology vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	CYP1A1 gene polymorphism and polycystic ovary syndrome. [electronic resource] by Esinler, Ibrahim Aktas, Dilek Otegen, Umit Alikasifoglu, Mehmet Yarali, Hakan Tuncbilek, Ergul Producer: 20080603 In: Reproductive biomedicine online vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Intrafamilial variability of XYLT2-related spondyloocular syndrome. [electronic resource] by Guleray, Naz Simsek Kiper, Pelin Ozlem Utine, Gulen Eda Boduroglu, Koray Alikasifoglu, Mehmet Producer: 20200206 In: European journal of medical genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Association of LOXL1 gene polymorphisms with exfoliation syndrome/glaucoma and primary open angle glaucoma in a Turkish population. [electronic resource] by Kasım, Burcu İrkeç, Murat Alikaşifoğlu, Mehmet Orhan, Mehmet Mocan, Mehmet Cem Aktaş, Dilek Producer: 20130906 In: Molecular vision vol. 19 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 68 results.