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	1.	DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis. [electronic resource] by Dinçer, P Topaloğlu, H Ayter, S Producer: 19981020 In: The Turkish journal of pediatrics vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	2.	Response (to Sewry and Goebel). [electronic resource] by Kayman-Kurekci, G Korkusuz, P Dincer, P Producer: 20150521 In: Neuromuscular disorders : NMD vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Good clinical observation is essential before molecular studies. [electronic resource] by Topaloglu, H Tan, E Dinçer, P Erdem, S Akçören, Z Producer: 19960102 In: Lancet (London, England) vol. 346 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	An unusual case of Duchenne muscular dystrophy. [electronic resource] by Topaloğlu, H Dinçer, P Göğüş, S Ayter, S Topçu, M Producer: 19931229 In: Brain & development vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients. [electronic resource] by Dinçer, P Topaloğlu, H Ayter, S Ozgüç, M Taşdemir, H A Renda, Y Producer: 19961105 In: Brain & development vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Prenatal diagnosis of limb-girdle muscular dystrophy type 2C. [electronic resource] by Dinçer, P Piccolo, F Leturcq, F Kaplan, J C Jeanpierre, M Topaloğlu, H Producer: 19990311 In: Prenatal diagnosis vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy. [electronic resource] by Taşdemir, H A Topaloğlu, H Dinçer, P Göğüş, S Kotiloğlu, E Ozdirim, E Yalaz, K Producer: 19971120 In: The Turkish journal of pediatrics vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	8.	A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F. [electronic resource] by Dinçer, P Bönnemann, C G Erdir Aker, O Akçoren, Z Nigro, V Kunkel, L M Topalolu, H Producer: 20000802 In: Neuromuscular disorders : NMD vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Effect of Vasoactive Therapy Used for Brain-Dead Donors on Graft Survival After Kidney Transplantation. [electronic resource] by Birtan, D Arslantas, M K Altun, G T Dincer, P C Gecegormez, S Demirel, A Ayanoglu, H O Producer: 20180928 In: Transplantation proceedings vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Calpain-3 deficiency causes a mild muscular dystrophy in childhood. [electronic resource] by Topaloğlu, H Dinçer, P Richard, I Akçören, Z Alehan, D Ozme, S Cağlar, M Karaduman, A Urtizberea, J A Beckmann, J S Producer: 19971125 In: Neuropediatrics vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Effect of Interviews Done by Intensive Care Physicians on Organ Donation. [electronic resource] by Birtan, D Arslantas, M K Dincer, P C Altun, G T Bilgili, B Ucar, F B Bozoklar, C A Ayanoglu, H O Producer: 20170529 In: Transplantation proceedings vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. [electronic resource] by Dinçer, P Akçören, Z Demir, E Richard, I Sancak, O Kale, G Ozme, S Karaduman, A Tan, E Urtizberea, J A Beckmann, J S Topaloğlu, H Producer: 20000717 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Beta-sarcoglycan gene mutations in Turkey. [electronic resource] by Balci, B Wilichowski, E Haliloğlu, G Talim, B Aurino, S Kremer, E Ebinger, F Senbil, N Anlar, B Kale, G Nigro, V Topaloğlu, H Bonnemann, C Dinçer, P Producer: 20051004 In: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	14.	A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. [electronic resource] by Dinçer, P Leturcq, F Richard, I Piccolo, F Yalnizoglu, D de Toma, C Akçören, Z Broux, O Deburgrave, N Brenguier, L Roudaut, C Urtizberea, J A Jung, D Tan, E Jeanpierre, M Campbell, K P Kaplan, J C Beckmann, J S Topaloglu, H Producer: 19970905 In: Annals of neurology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins. [electronic resource] by Richard, I Brenguier, L Dinçer, P Roudaut, C Bady, B Burgunder, J M Chemaly, R Garcia, C A Halaby, G Jackson, C E Kurnit, D M Lefranc, G Legum, C Loiselet, J Merlini, L Nivelon-Chevallier, A Ollagnon-Roman, E Restagno, G Topaloglu, H Beckmann, J S Producer: 19970603 In: American journal of human genetics vol. 60 Availability: No items available. Save to lists Add to cart (remove)
	16.	Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies. [electronic resource] by Beckmann, J S Richard, I Broux, O Fougerousse, F Allamand, V Chiannilkulchai, N Lim, L E Duclos, F Bourg, N Brenguier, L Pasturaud, P Quétier, F Roudaut, C Sunada, Y Meyer, J Dinçer, P Lefranc, G Merlini, L Topaloglu, H Tomé, F M Cohen, D Jackson, C E Campbell, K P Fardeau, M Producer: 19970508 In: Neuromuscular disorders : NMD vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)