Your search returned 21 results.

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	1.	Orthostatic heart rate variability analysis in idiopathic Parkinson's disease. [electronic resource] by Mihci, E Kardelen, F Dora, B Balkan, S Producer: 20060628 In: Acta neurologica Scandinavica vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13). [electronic resource] by Cetin, Z Mihci, E Keser, I Luleci, G Producer: 20120828 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	3.	Selective IgM deficiency in a boy with ring chromosome 18. [electronic resource] by Celmeli, F Turkkahraman, D Cetin, Z Mihci, E Yegin, O Producer: 20150316 In: Journal of investigational allergology & clinical immunology vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	4.	Double partial trisomy of 6p23-pter and 9pter-q21.2 in a neonate resulting from 4:2 meiotic segregation of a maternal complex t(6;7;9)(p23;p15;q21.2) translocation. [electronic resource] by Cetin, Z Mihci, E Keser, I Karaali, K Berker, S Luleci, G Producer: 20120828 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	5.	Interstitial deletion of 13q22-q32: a case with choanal atresia and mega-cisterna magna and review of the literature. [electronic resource] by Cetin, Z Mihci, E Yakut, S Karaali, K Luleci, G Keser, I Producer: 20111123 In: Genetic counseling (Geneva, Switzerland) vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	6.	Molecular analysis of fragile X syndrome in Antalya Province. [electronic resource] by Bilgen, T Keser, I Mihci, E Haspolat, S Tacoy, S Luleci, G Producer: 20050621 In: Indian journal of medical sciences vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	7.	C.428_451 dup(24bp) mutation of the ARX gene detected in a Turkish family. [electronic resource] by Arikan, Y Bilgen, T Koken, R Turan, S Mihci, E Keser, I Producer: 20121120 In: Genetic counseling (Geneva, Switzerland) vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	8.	Comprehensive dental management in a Hallermann-Streiff syndrome patient with unusual radiographic appearance of teeth. [electronic resource] by Gungor, O Erken Nur, B Guzel Yalcin, H Karayilmaz, H Mihci, E Producer: 20160324 In: Nigerian journal of clinical practice vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features. [electronic resource] by Caliskan, M O Karauzum, S B Mihci, E Tacoy, S Luleci, G Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	10.	De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome. [electronic resource] by Yakut, S Cetin, Z Berker-Karauzum, S Mihci, E Mendilcioglu, I Luleci, G Producer: 20110711 In: Genetic counseling (Geneva, Switzerland) vol. 22 Availability: No items available. Save to lists Add to cart (remove)
	11.	A case with de novo interstitial deletion of chromosome 7q21.1-q22. [electronic resource] by Manguoğlu, E Berker-Karaüzüm, S Baumer, A Mihçi, E Taçoy, S Lüleci, G Schinzel, A Producer: 20060111 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	12.	22q11.2 syndrome due to maternal translocation t(18;22) (pl1.2;q11.2). [electronic resource] by Nur, B G Cetin, Z Clark, O A Mihci, E Oygur, N Karauzum, S B Producer: 20150619 In: Genetic counseling (Geneva, Switzerland) vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	13.	A MOLECULARLY CHARACTERIZED INTERSTITIAL DELETION ENCOMPASSING THE 11q14.1-q23.3 REGION IN A CASE WITH MULTIPLE CONGENITAL ABNORMALITIES. [electronic resource] by Cetin, Z Altiok-Clark, O Yakut, S Guzel-Nur, B Mihci, E Berker-Karauzum, S Producer: 20160607 In: Genetic counseling (Geneva, Switzerland) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	14.	Mosaic Intrachromosomal Triplication of (12)(p11.2p13) in a Patient with Pallister-Killian Syndrome. [electronic resource] by Yakut, S Mihci, E Altiok Clark, O Cetin, Z Keser, I Berker, S Luleci, G Producer: 20130920 In: Balkan journal of medical genetics : BJMG vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	The clinical spectrum of a rare chromosomal abnormality: Isochromosome 18p. [electronic resource] by Nur, B G Clark, O A Cetin, Z Toylu, A Karauzum, S B Mihci, E Producer: 20180315 In: Genetic counseling (Geneva, Switzerland) vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	16.	Persistent hyperinsulinaemic hypoglycaemia of infancy: case report. [electronic resource] by Semiz, S Bircan, I Akçurin, S Mihçi, E Melikoglu, M Karagüzel, G Kiliçaslan, B Karpuzoğlu, G Producer: 20030328 In: East African medical journal vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	[Influence of percutaneous coronary intervention in non ST-elevation acute coronary syndromes on prescription of secondary prevention medications. Data from the S-Témoin Registry]. [electronic resource] by Danchin, N Thébaut, J F Diévart, F Grenier, O Mihci, E Herrmann, M A Ferrières, J Producer: 20070403 In: Annales de cardiologie et d'angeiologie vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	M-FISH applications in clinical genetics. [electronic resource] by Cetin, Z Berker Karaüzüm, S Yakut, S Mihçi, E Baumer, A Wey, E Taçoy, S Bağci, G Lüleci, G Producer: 20060215 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	19.	Progressive symmetrical erythrokeratoderma: report of a Turkish family and evaluation for loricrin and connexin gene mutations. [electronic resource] by Akman, A Masse, M Mihci, E Richard, G Christiano, A M Balle, B J Ciftcioglu, M A Alpsoy, E Producer: 20081210 In: Clinical and experimental dermatology vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Prevalence of peripheral arterial disease in high-risk patients using ankle-brachial index in general practice: a cross-sectional study. [electronic resource] by Cacoub, P Cambou, J-P Kownator, S Belliard, J-P Beregi, J-P Branchereau, A Carpentier, P Léger, P Luizy, F Maïza, D Mihci, E Herrmann, M-A Priollet, P Producer: 20090515 In: International journal of clinical practice vol. 63 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 21 results.