Your search returned 29 results.

Results
	1.	Autosomal Recessive Oculodentodigital Dysplasia: A Case Report and Review of the Literature. [electronic resource] by Taşdelen, Elifcan Durmaz, Ceren D Karabulut, Halil G Producer: 20180724 In: Cytogenetic and genome research vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The role of thrombofilia related to Factor V Leiden and Factor II G20210A mutations in recurrent abortions. [electronic resource] by Aksoy, Muge Tek, Ibrahim Karabulut, Halil Berker, Bulent Soylemez, Feride Producer: 20050621 In: JPMA. The Journal of the Pakistan Medical Association vol. 55 Availability: No items available. Save to lists Add to cart (remove)
	3.	Thymidylate synthase genetic polymorphism and plasma total homocysteine level in a group of Turkish patients with rheumatoid arthritis: relationship with disease activity and methotrexate toxicity. [electronic resource] by Borman, Pınar Taşbaş, Özgur Karabulut, Halil Tukun, Ajlan Yorgancıoğlu, Rezan Producer: 20180515 In: Revista brasileira de reumatologia vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A Novel PORCN Frameshift Mutation Leading to Focal Dermal Hypoplasia: A Case Report. [electronic resource] by Durmaz, Ceren D McGrath, John Liu, Lu Karabulut, Halil G Producer: 20180530 In: Cytogenetic and genome research vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The Frequency of A1298C and C677T Polymorphisms of the Methylentetrahydrofolate Gene in Turkish Patients with Rheumatoid Arthritis: Relationship with Methotrexate Toxicity. [electronic resource] by Taşbaş, Ozgür Borman, Pınar Gürhan Karabulut, Halil Tükün, Ajlan Yorgancıoğlu, Rezan Producer: 20111110 In: The open rheumatology journal vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Factor V Leiden and prothrombin gene G20210A mutations in ocular Behçet disease. [electronic resource] by Batioğlu, Figen Atmaca, Leyla S Karabulut, Halil Gürhan Beyza Sayin, Derya Producer: 20031002 In: Acta ophthalmologica Scandinavica vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	DNA methyltransferase expression differs with proliferation in childhood acute lymphoblastic leukemia. [electronic resource] by Sayin, Derya Beyza Kürekçi, Emin Karabulut, Halil Gürhan Ezer, Ustün Bökesoy, Isik Producer: 20100930 In: Molecular biology reports vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Alpha-1 Antitrypsin Levels and Polymorphisms in Interstitial Lung Diseases. [electronic resource] by Demir, Nalan Erçen Diken, Özlem Karabulut, Halil Gürhan Karnak, Demet Kayacan, Oya Producer: 20181224 In: Turkish journal of medical sciences vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Extending Phenotypic Spectrum of 17q22 Microdeletion: Growth Hormone Deficiency. [electronic resource] by Durmaz, Ceren Damla Altıner, Şule Taşdelen, Elifcan Karabulut, Halil Gürhan Ruhi, Hatice Ilgın Producer: 20211007 In: Fetal and pediatric pathology vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy. [electronic resource] by Cabuk, Feryal Karabulut, Halil G Tuncali, Timur Karademir, Selmin Bozdayi, Mithat Tükün, Ajlan Producer: 20070524 In: The Turkish journal of pediatrics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	11.	The 8p11 myeloproliferative syndrome in a 3-year-old child. [electronic resource] by Kuskonmaz, Baris Kafali, Candas Akcoren, Zuhal Karabulut, Halil G Akalin, Ibrahim Tuncer, Murat A Producer: 20080303 In: Leukemia research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Y-STR polymorphism in Central Anatolian Region of Turkey. [electronic resource] by Rustamov, Aydin Gümüş, Güvem Karabulut, Halil Gürhan Elhan, Atilla Halil Kadikiran, Ahmet Bökesoy, Işik Producer: 20040527 In: Forensic science international vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Endothelial nitric oxide synthase gene intron 4 polymorphism predicts new onset diabetes mellitus after transplantation in kidney allograft recipients treated with cyclosporin A. [electronic resource] by Ergün, Ihsan Keven, Kenan Sengül, Sule Karabulut, Halil Gürhan Kurultak, Ilhan Soypacaci, Zeki Erbay, Bülent Producer: 20110923 In: International urology and nephrology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	CYP1A1, GST gene polymorphisms and risk of chronic myeloid leukemia. [electronic resource] by Taspinar, Mehmet Aydos, Sena Erdogan Comez, Omer Elhan, Atilla Halil Karabulut, Halil Gurhan Sunguroglu, Asuman Producer: 20080429 In: Swiss medical weekly vol. 138 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Association Between N363S and BclI Polymorphisms of the Glucocorticoid Receptor Gene (NR3C1) and Glucocorticoid Side Effects During Childhood Acute Lymphoblastic Leukemia Treatment. [electronic resource] by Kaymak Cihan, Meriç Karabulut, Halil Gürhan Yürür Kutlay, Nüket Ilgın Ruhi, Hatice Tükün, Ajlan Olcay, Lale Producer: 20180208 In: Turkish journal of haematology : official journal of Turkish Society of Haematology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Primary Hypertrophic Osteoarthropathy Mimicking Juvenile Idiopathic Arthritis: A Novel SLCO2A1 Mutation and Imaging Findings. [electronic resource] by Torgutalp, Murat Durmaz, Ceren D Karabulut, Halil G Seifert, Wenke Horn, Denise Akkaya, Zehra Turgay, Murat Producer: 20190905 In: Cytogenetic and genome research vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	ACE gene deletion/deletion polymorphism may be a protective factor for respiratory distress in preterm infants. [electronic resource] by Sivasli, Ercan Yurdakök, Murat Babaoğlu, Elif Karabulut, Halil Yiğit, Sule Babaoğlu, Melih Tekinalp, Gülsevin Tükün, Ajlan Producer: 20070524 In: The Turkish journal of pediatrics vol. 49 Availability: No items available. Save to lists Add to cart (remove)
	18.	The impact of vitamin D receptor genotype on the management of anemia in hemodialysis patients. [electronic resource] by Ertürk, Sehsuvar Kutlay, Sim Karabulut, Halil G Keven, Kenan Nergizoglu, Gökhan Ates, Kenan Bokesoy, Isik Duman, Neval Producer: 20021017 In: American journal of kidney diseases : the official journal of the National Kidney Foundation vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature. [electronic resource] by Delil, Kenan Karabulut, Halil Gürhan Hacıhamdioğlu, Bülent Şıklar, Zeynep Berberoğlu, Merih Öçal, Gönül Tükün, Ajlan Ruhi, Hatice Ilgın Producer: 20170412 In: Journal of clinical research in pediatric endocrinology vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome. [electronic resource] by Altiner, Şule Karabulut, Halil G Yararbaş, Kanay Tükün, Ajlan Collet, Corinne Kocaay, Pinar Berberoğlu, Merih Ilgin Ruhi, Hatice Producer: 20180827 In: Clinical dysmorphology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 29 results.