Your search returned 33 results.

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	1.	Multiplex ligation-dependent probe amplification is superior for detecting deletions/duplications in Duchenne muscular dystrophy. [electronic resource] by Schwartz, M Dunø, M Producer: 20050524 In: Clinical genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Becker muscular dystrophy with widespread muscle hypertrophy and a non-sense mutation of exon 2. [electronic resource] by Witting, N Duno, M Vissing, J Producer: 20130904 In: Neuromuscular disorders : NMD vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Leukocyte cDNA analysis of NSD1 derived from confirmed Sotos syndrome patients. [electronic resource] by Duno, M Skovby, F Schwartz, M Producer: 20071219 In: Annals of human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Targeted deletions created in yeast vectors by recombinational excision. [electronic resource] by Dunø, M Bendixen, C Krejci, L Thomsen, B Producer: 20050829 In: Nucleic acids research vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	5.	Genetic dissection of intersubunit contacts within human protein kinase CK2. [electronic resource] by Kusk, M Bendixen, C Dunø, M Westergaard, O Thomsen, B Producer: 19951226 In: Journal of molecular biology vol. 253 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Genetic analysis of the Saccharomyces cerevisiae Sgs1 helicase defines an essential function for the Sgs1-Top3 complex in the absence of SRS2 or TOP1. [electronic resource] by Dunø, M Thomsen, B Westergaard, O Krejci, L Bendixen, C Producer: 20001026 In: Molecular & general genetics : MGG vol. 264 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort. [electronic resource] by Nielsen, T T Svenstrup, K Duno, M Nielsen, J E Producer: 20140825 In: Spinal cord vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Molecular dissection of interactions between Rad51 and members of the recombination-repair group. [electronic resource] by Krejci, L Damborsky, J Thomsen, B Duno, M Bendixen, C Producer: 20010208 In: Molecular and cellular biology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy. [electronic resource] by Ostergaard, E Batbayli, M Duno, M Vilhelmsen, K Rosenberg, T Producer: 20110128 In: Journal of medical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Homomeric interaction of the mouse Rad52 protein. [electronic resource] by Krejci, L Thomsen, B Duno, M Westergaard, O Bendixen, C Producer: 20010108 In: Molecular biology reports vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Xanthurenic aciduria due to a mutation in KYNU encoding kynureninase. [electronic resource] by Christensen, M Duno, M Lund, A M Skovby, F Christensen, E Producer: 20070426 In: Journal of inherited metabolic disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel arginine-to-cysteine substitution in the triple helical region of the alpha1(I) collagen chain in a family with an osteogenesis imperfecta/Ehlers-Danlos phenotype. [electronic resource] by Lund, Am Joensen, F Christensen, E Dunø, M Skovby, F Schwartz, M Producer: 20080229 In: Clinical genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Muscle regeneration in mitochondrial myopathies. [electronic resource] by Krag, T O Hauerslev, S Jeppesen, T D Duno, M Vissing, J Producer: 20130827 In: Mitochondrion vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Endocrine function in 97 patients with myotonic dystrophy type 1. [electronic resource] by Ørngreen, M C Arlien-Søborg, P Duno, M Hertz, J M Vissing, J Producer: 20121017 In: Journal of neurology vol. 259 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Mitochondrial dysfunction and risk of cancer. [electronic resource] by Lund, M Melbye, M Diaz, L J Duno, M Wohlfahrt, J Vissing, J Producer: 20150513 In: British journal of cancer vol. 112 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Primary failure of eruption of teeth in two siblings with a novel mutation in the PTH1R gene. [electronic resource] by Aziz, S Hermann, N V Dunø, M Risom, L Daugaard-Jensen, J Kreiborg, S Producer: 20191029 In: European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Short- and long-term effects of endurance training in patients with mitochondrial myopathy. [electronic resource] by Jeppesen, T D Dunø, M Schwartz, M Krag, T Rafiq, J Wibrand, F Vissing, J Producer: 20100202 In: European journal of neurology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A new mutation of the fukutin gene causing late-onset limb girdle muscular dystrophy. [electronic resource] by Riisager, M Duno, M Hansen, F Juul Krag, T O Vissing, C R Vissing, J Producer: 20140213 In: Neuromuscular disorders : NMD vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case report. [electronic resource] by Juul, A Aksglaede, L Lund, A M Duno, M Skakkebaek, N E Rajpert-De Meyts, E Producer: 20070926 In: Human reproduction (Oxford, England) vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Multiple mtDNA deletions with features of MNGIE. [electronic resource] by Vissing, J Ravn, K Danielsen, E R Dunø, M Wibrand, F Wevers, R A Schwartz, M Producer: 20021016 In: Neurology vol. 59 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 33 results.