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	1781.	Secondary medical diagnosis in fragile X syndrome with and without autism spectrum disorder. [electronic resource] by García-Nonell, Catalina Ratera, Eugenia Rigau Harris, Susan Hessl, David Ono, Michele Y Tartaglia, Nicole Marvin, Emily Tassone, Flora Hagerman, Randi J Producer: 20080819 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1782.	Influence of androgen receptor repeat polymorphisms on personality traits in men. [electronic resource] by Westberg, Lars Henningsson, Susanne Landén, Mikael Annerbrink, Kristina Melke, Jonas Nilsson, Staffan Rosmond, Roland Holm, Göran Anckarsäter, Henrik Eriksson, Elias Producer: 20090730 In: Journal of psychiatry & neuroscience : JPN vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	1783.	Quadruplex-forming properties of FRAXA (CGG) repeats interrupted by (AGG) triplets. [electronic resource] by Renciuk, Daniel Zemánek, Michal Kejnovská, Iva Vorlícková, Michaela Producer: 20090414 In: Biochimie vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1784.	Progression rate of neurological deficits in a 10-year cohort of SCA3 patients. [electronic resource] by Jardim, Laura Bannach Hauser, Lisiane Kieling, Christian Saute, Jonas Alex Morales Xavier, Renan Rieder, Carlos Roberto Mello Monte, Thais Lampert Camey, Suzi Torman, Vanessa Bielefeld Leotti Producer: 20110125 In: Cerebellum (London, England) vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1785.	Structural insights into CUG repeats containing the 'stretched U-U wobble': implications for myotonic dystrophy. [electronic resource] by Kiliszek, Agnieszka Kierzek, Ryszard Krzyzosiak, Wlodzimierz J Rypniewski, Wojciech Producer: 20090805 In: Nucleic acids research vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1786.	Neuropathology and therapeutic intervention in spinal and bulbar muscular atrophy. [electronic resource] by Banno, Haruhiko Katsuno, Masahisa Suzuki, Keisuke Tanaka, Fumiaki Sobue, Gen Producer: 20140415 In: International journal of molecular sciences vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1787.	Historical determinants of contemporary attributes of African descendants in the Americas: the androgen receptor holds the key. [electronic resource] by Aiken, W D Producer: 20120306 In: Medical hypotheses vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1788.	Huntington's disease: fighting on many fronts. [electronic resource] by Andre, Ralph Wild, Edward J Tabrizi, Sarah J Producer: 20120608 In: Brain : a journal of neurology vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1789.	Beyond the GWAS in schizophrenia. [electronic resource] by Malhotra, Anil K Producer: 20111003 In: EMBO molecular medicine vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1790.	The unstable repeats--three evolving faces of neurological disease. [electronic resource] by Nelson, David L Orr, Harry T Warren, Stephen T Producer: 20130422 In: Neuron vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1791.	AGG/CCT interruptions affect nucleosome formation and positioning of healthy-length CGG/CCG triplet repeats. [electronic resource] by Volle, Catherine B Delaney, Sarah Producer: 20140617 In: BMC biochemistry vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1792.	ATXN2 trinucleotide repeat length correlates with risk of ALS. [electronic resource] by Sproviero, William Shatunov, Aleksey Stahl, Daniel Shoai, Maryam van Rheenen, Wouter Jones, Ashley R Al-Sarraj, Safa Andersen, Peter M Bonini, Nancy M Conforti, Francesca L Van Damme, Philip Daoud, Hussein Del Mar Amador, Maria Fogh, Isabella Forzan, Monica Gaastra, Ben Gellera, Cinzia Gitler, Aaron D Hardy, John Fratta, Pietro La Bella, Vincenzo Le Ber, Isabelle Van Langenhove, Tim Lattante, Serena Lee, Yi-Chung Malaspina, Andrea Meininger, Vincent Millecamps, Stéphanie Orrell, Richard Rademakers, Rosa Robberecht, Wim Rouleau, Guy Ross, Owen A Salachas, Francois Sidle, Katie Smith, Bradley N Soong, Bing-Wen Sorarù, Gianni Stevanin, Giovanni Kabashi, Edor Troakes, Claire van Broeckhoven, Christine Veldink, Jan H van den Berg, Leonard H Shaw, Christopher E Powell, John F Al-Chalabi, Ammar Producer: 20170928 In: Neurobiology of aging vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1793.	Polymorphisms in the androgen receptor CAG repeat sequence are related to tumour stage but not to ERG or androgen receptor expression in Malaysian men with prostate cancer. [electronic resource] by Tan, J S J Ong, K C Ong, D B L Wu, Y S Razack, A Kuppusamy, S Lim, J Rhodes, A Producer: 20200623 In: The Malaysian journal of pathology vol. 41 Availability: No items available. Save to lists Add to cart (remove)
	1794.	Chromosome-specific panels of tri- and tetranucleotide microsatellite markers for multiplex fluorescent detection and automated genotyping: evaluation of their utility in pathology and forensics. [electronic resource] by Lindqvist, A K Magnusson, P K Balciuniene, J Wadelius, C Lindholm, E Alarcón-Riquelme, M E Gyllensten, U B Producer: 19970320 In: Genome research vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1795.	Evidence for genetic anticipation in the oculodentodigital syndrome. [electronic resource] by Shapiro, R E Griffin, J W Stine, O C Producer: 19970904 In: American journal of medical genetics vol. 71 Availability: No items available. Save to lists Add to cart (remove)
	1796.	Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization. [electronic resource] by Haaf, T Sirugo, G Kidd, K K Ward, D C Producer: 19960305 In: Nature genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1797.	An interrupted 34-CAG repeat SCA-2 allele in patients with sporadic spinocerebellar ataxia. [electronic resource] by Costanzi-Porrini, S Tessarolo, D Abbruzzese, C Liguori, M Ashizawa, T Giacanelli, M Producer: 20000218 In: Neurology vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1798.	Restless legs syndrome in spinocerebellar ataxia types 1, 2, and 3. [electronic resource] by Abele, M Bürk, K Laccone, F Dichgans, J Klockgether, T Producer: 20011004 In: Journal of neurology vol. 248 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1799.	Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles. [electronic resource] by Dombrowski, C Lévesque, S Morel, M L Rouillard, P Morgan, K Rousseau, F Producer: 20020709 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1800.	NGG-triplet repeats form similar intrastrand structures: implications for the triplet expansion diseases. [electronic resource] by Usdin, K Producer: 19981015 In: Nucleic acids research vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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