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	1.	Hereditary Neuropathy with Liability to Pressure Palsies Masked by Previous Gunshots and Tuberculosis. [electronic resource] by Gencik, Martin Finsterer, Josef Producer: 20151207 In: Case reports in genetics vol. 2015 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The relevance of the individual genetic background for the toxicokinetics of two significant neurodevelopmental toxicants: mercury and lead. [electronic resource] by Gundacker, Claudia Gencik, Martin Hengstschläger, Markus Producer: 20101105 In: Mutation research vol. 705 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	On the genetic contribution to selected multifactorial diseases with autoimmune characteristics. [electronic resource] by Miterski, Bianca Epplen, Jörg T Gencik, Martin Producer: 20030805 In: Cellular and molecular biology (Noisy-le-Grand, France) vol. 48 Availability: No items available. Save to lists Add to cart (remove)
	4.	On the edge of noncompaction: minimally manifesting Duchenne carrier due to the dystrophin mutation n.2867A>C. [electronic resource] by Finsterer, Josef Stöllberger, Claudia Vlckova, Zoja Gencik, Martin Producer: 20140207 In: International journal of cardiology vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Familial accumulation of sudden cardiac deaths and the LMNA variant c.868G>A (p.Glu290Lys). [electronic resource] by Finsterer, Josef Stöllberger, Claudia Keller, Hans Gencik, Martin Producer: 20170807 In: International journal of cardiology vol. 215 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Noncompaction predisposing for recurrent Takotsubo syndrome in myotonic dystrophy 1. [electronic resource] by Finsterer, Josef Stöllberger, Claudia Hornykewycz, Anette Gencik, Martin Producer: 20140530 In: International journal of cardiology vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	First IKBKG gene mutation study in Serbian incontinentia pigmenti patients. [electronic resource] by Minić, Snezana Trpinac, Dusan Gabriel, Heinz Gencik, Martin Obradović, Miljana Producer: 20151106 In: Srpski arhiv za celokupno lekarstvo vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Dental and oral anomalies in incontinentia pigmenti: a systematic review. [electronic resource] by Minić, Snežana Trpinac, Dušan Gabriel, Heinz Gencik, Martin Obradović, Miljana Producer: 20140109 In: Clinical oral investigations vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	A novel nonsense autosomal dominant mutation in the GLRA1 gene causing hyperekplexia. [electronic resource] by Milenkovic, Ivan Zimprich, Alexander Gencik, Martin Platho-Elwischger, Kirsten Seidel, Stefan Producer: 20191114 In: Journal of neural transmission (Vienna, Austria : 1996) vol. 125 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Polymorphisms of the tumor necrosis factor receptors: no association with narcolepsy in German patients. [electronic resource] by Wieczorek, Stefan Dahmen, Norbert Jagiello, Peter Epplen, Joerg T Gencik, Martin Producer: 20031104 In: Journal of molecular medicine (Berlin, Germany) vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Rapidly progressive phenotype of Lafora disease associated with a novel NHLRC1 mutation. [electronic resource] by Brackmann, Florian A Kiefer, Alexander Agaimy, Abbas Gencik, Martin Trollmann, Regina Producer: 20120328 In: Pediatric neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Non-lethal non-mosaic male with Conradi-Hunermann syndrome caused by a novel EBP c.356T>G mutation. [electronic resource] by Bode, Harald Galm, Christoph Hummler, Helmut Teller, Christopher Haas, Dorothea Gencik, Martin Producer: 20140326 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Recurrent takotsubo syndrome in a patient with myotonic dystrophy 1. [electronic resource] by Finsterer, Josef Stöllberger, Claudia Demirtas, Dita Gencik, Martin Ohnutek, Irene Hornykewycz, Anette Producer: 20150415 In: Acute cardiac care vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Syncope and hyperCKemia as minimal manifestations of short CTG repeat expansions in myotonic dystrophy type 1. [electronic resource] by Finsterer, Josef Stöllberger, Claudia Gencik, Martin Höftberger, Romana Rahimi, Jasmin Mokocki, Johannes Producer: 20170419 In: Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Genetic background of lead and mercury metabolism in a group of medical students in Austria. [electronic resource] by Gundacker, Claudia Wittmann, Karl J Kukuckova, Martina Komarnicki, Günter Hikkel, Imrich Gencik, Martin Producer: 20090717 In: Environmental research vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	A novel PANK2 gene mutation: clinical and molecular characteristics of patients short communication. [electronic resource] by Kazek, Beata Jamroz, Ewa Gencik, Martin Jezela Stanek, Aleksandra Marszal, Elzbieta Wojaczynska-Stanek, Katarzyna Producer: 20080214 In: Journal of child neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Cochlear Implantation in Siblings With Refsum's Disease. [electronic resource] by Stähr, Kerstin Kuechler, Alma Gencik, Martin Arnolds, Judith Dendy, Meaghan Lang, Stephan Arweiler-Harbeck, Diana Producer: 20170821 In: The Annals of otology, rhinology, and laryngology vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Brachytelephalangic chondrodysplasia punctata with a new hemizygous missense mutation in a neonate. [electronic resource] by Meyer, Sascha Löffler, Günther Gencik, Martin Fries, Peter Papanagiotou, Panagiotis Oehl-Jaschkowitz, Barbara Gortner, Ludwig Producer: 20130805 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Glutathione-S-transferase polymorphism, metallothionein expression, and mercury levels among students in Austria. [electronic resource] by Gundacker, Claudia Komarnicki, Günter Jagiello, Peter Gencikova, Alexandra Dahmen, Norbert Wittmann, Karl J Gencik, Martin Producer: 20071108 In: The Science of the total environment vol. 385 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	The Lebanese Allele in the [electronic resource] by Mansour, Hicham Sabbagh, Sandra Bizzari, Sami El-Hayek, Stephany Chouery, Eliane Gambarini, Alicia Gencik, Martin Mégarbané, André Publication details: Journal of pediatric genetics Sep 2019 In: Journal of pediatric genetics vol. 8 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 26 results.