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	1.	Neural tube defects in Turkey: prevalence, distribution and risk factors. [electronic resource] by Tunçbilek, E Boduroğlu, K Alikaşifoğlu, M Producer: 20000516 In: The Turkish journal of pediatrics vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	2.	Dyskeratosis congenita with an unusual chromosomal abnormality. [electronic resource] by Demiroglŭ, H Alikaşifoğlu, M Dündar, S Producer: 19970619 In: British journal of haematology vol. 97 Availability: No items available. Save to lists Add to cart (remove)
	3.	Results of the Turkish congenital malformation survey. [electronic resource] by Tunçbilek, E Boduroğlu, K Alikaşifoğlu, M Producer: 20000516 In: The Turkish journal of pediatrics vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	4.	Aplastic anaemia and reticulated skin hyperpigmentation. [electronic resource] by Demiroğlu, H Alikaşifoğlu, M Yalçin, B Dündar, S Producer: 19980324 In: Postgraduate medical journal vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Ring chromosome 13 in an infant with multiple congenital anomalies and penoscrotal transposition. [electronic resource] by Boduroglu, K Alikaşifoglu, M Tunçbilek, E Uludogan, S Producer: 19990208 In: Clinical dysmorphology vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	677-->CT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey. [electronic resource] by Boduroglu, K Alikasifoglu, M Anar, B Tuncbilek, E Producer: 19980827 In: Archives of disease in childhood. Fetal and neonatal edition vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Chest wall abscess as an unusual presentation of childhood tuberculosis. [electronic resource] by Taşdan, Y Alikaşifoğlu, M Midilli, K Ilter, O Producer: 19980312 In: The Pediatric infectious disease journal vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. [electronic resource] by Boduroğlu, K Alikaşifoğlu, M Anar, B Tunçbilek, E Producer: 19990525 In: Journal of child neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Brucella osteomyelitis of the calcaneus. [electronic resource] by Taşdan, Y Alikaşifoğlu, M Midilli, K Ilter, O Producer: 19980929 In: The Pediatric infectious disease journal vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Thermolabile methylenetetrahydrofolate reductase enzyme genotype is frequent in type 2 diabetic patients with normal fasting homocysteine levels. [electronic resource] by Tutuncu, N B Erbas, T Alikasifoglu, M Tuncbilek, E Producer: 20050526 In: Journal of internal medicine vol. 257 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Acute lymphoblastic leukemia associated with Klinefelter syndrome. [electronic resource] by Gürgey, A Kara, A Tuncer, M Alikaşifoğlu, M Tunçbilek, E Producer: 19940712 In: Pediatric hematology and oncology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Genetic linkage analysis of autosomal dominant polycystic kidney disease in a Turkish family. [electronic resource] by Sungur, C Alikaşifoglu, M Breuning, M H Peters, D J Producer: 19951213 In: Nephron vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	CYP1A1 gene polymorphism and risk of endometrial hyperplasia and endometrial carcinoma. [electronic resource] by Esinler, I Aktas, D Alikasifoglu, M Tuncbilek, E Ayhan, A Producer: 20070227 In: International journal of gynecological cancer : official journal of the International Gynecological Cancer Society vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology. [electronic resource] by Tunçbilek, E Alikasifoğlu, M Boduroğlu, K Aktas, D Anar, B Producer: 19990624 In: American journal of medical genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Iron status in breast-fed full-term infants. [electronic resource] by Arvas, A Elgörmüş, Y Gür, E Alikaşifoğlu, M Celebi, A Producer: 20000412 In: The Turkish journal of pediatrics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	16.	Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family. [electronic resource] by Koc, A Pronk, J C Alikasifoglu, M Joenje, H Altay, C Producer: 19990322 In: British journal of haematology vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Coexistent mosaic monosomy 21 and fragile X syndrome in a mentally retarded male patient. [electronic resource] by Utine, G E Aktas, D Boduroğlu, K Alikasifoğlu, M Tunçbilek, E Producer: 20071016 In: Genetic counseling (Geneva, Switzerland) vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	18.	TWO CASES WITH DIFFERENT EPILEPSY TYPE AND DYSMORPHIC FEATURES ASSOCIATED WITH 17q21.31 MICRODELETION SYNDROME. [electronic resource] by Uctepe, E Aktas, D Alikasifoglu, M Gunduz, E Sonmez, F M Producer: 20181016 In: Genetic counseling (Geneva, Switzerland) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	19.	Microdeletion of 22q11 (CATCH 22) in children with conotruncal heart defect and extracardiac malformations. [electronic resource] by Alikaşifoğlu, M Malkoç, N Ceviz, N Ozme, S Uludoğan, S Tunçbilek, E Producer: 20001228 In: The Turkish journal of pediatrics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	20.	Effects of angiotensin-converting enzyme gene polymorphism on the left-ventricular function and mass in patients with acromegaly. [electronic resource] by Erbas, T Alikasifoglu, M Aksöyek, S Unsal, I Gedik, O Tuncbilek, E Producer: 20000718 In: Cardiology vol. 92 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 48 results.