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	841.	Molecular analysis of Fragile X syndrome. [electronic resource] by Basehore, Monica J Friez, Michael J Producer: 20091127 In: Current protocols in human genetics vol. Chapter 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	842.	A case report of exhibitionist behaviour revealing unsuspected Huntington's disease: a pitfall in forensic medicine. [electronic resource] by Mondon, Karl Beaufils, Emilie Marqué, Aurélie de Toffol, Bertrand Constans, Thierry Hommet, Caroline Producer: 20090127 In: Journal of forensic and legal medicine vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	843.	MICA*055: a new allele with eight GCT repeats in the exon 5 microsatellite. [electronic resource] by Glas, J Maier, K Wetzke, M Henninger, M Weiss, E H Folwaczny, M Producer: 20090518 In: Tissue antigens vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	844.	Association of androgen receptor CAG repeat polymorphism and polycystic ovary syndrome. [electronic resource] by Shah, Nissar A Antoine, Heath J Pall, Marita Taylor, Kent D Azziz, Ricardo Goodarzi, Mark O Producer: 20080617 In: The Journal of clinical endocrinology and metabolism vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	845.	Crystallographic characterization of CCG repeats. [electronic resource] by Kiliszek, Agnieszka Kierzek, Ryszard Krzyzosiak, Wlodzimierz J Rypniewski, Wojciech Producer: 20121123 In: Nucleic acids research vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	846.	[Juvenile Huntington disease: A case study]. [electronic resource] by Nejjari, I Rhouda, H Bouhouche, A Kriouile, Y Producer: 20140612 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	847.	[Analysis of AGG interspersion of the FMR1 gene in fragile X syndrome]. [electronic resource] by Tang, Lifang Xiao, Bing Xu, Yan Ji, Xing Jiang, Wenting Liu, Xiaoqing Tao, Jiong Producer: 20150616 In: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	848.	Environmental Stress Induces Trinucleotide Repeat Mutagenesis in Human Cells by Alt-Nonhomologous End Joining Repair. [electronic resource] by Chatterjee, Nimrat Lin, Yunfu Yotnda, Patricia Wilson, John H Producer: 20170609 In: Journal of molecular biology vol. 428 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	849.	A dynamic trinucleotide repeat (TNR) expansion in the DMD gene. [electronic resource] by Kekou, Kyriaki Sofocleous, Christalena Papadimas, George Petichakis, Dimitris Svingou, Maria Pons, Roser-Maria Vorgia, Pelagia Gika, Artemis Kitsiou-Tzeli, Sophia Kanavakis, Emmanuel Producer: 20171113 In: Molecular and cellular probes vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	850.	Monitoring Double-Strand Break Repair of Trinucleotide Repeats Using a Yeast Fluorescent Reporter Assay. [electronic resource] by Poggi, Lucie Dumas, Bruno Richard, Guy-Franck Producer: 20201117 In: Methods in molecular biology (Clifton, N.J.) vol. 2056 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	851.	Myotonic dystrophy and cardiac disorders. [electronic resource] by Rakocević-Stojanović, V Grujić, M Seferović, P Lavrnić, D Pavlovic, S Nesković, V Romac, S Apostolski, S Producer: 20010419 In: Panminerva medica vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	852.	Association of oestrogen receptor alpha polymorphisms and androgen receptor CAG trinucleotide repeats with male infertility: a study in 109 Greek infertile men. [electronic resource] by Kukuvitis, A Georgiou, I Bouba, I Tsirka, A Giannouli, C H Yapijakis, C Tarlatzis, B Bontis, J Lolis, D Sofikitis, N Papadimas, J Producer: 20020927 In: International journal of andrology vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	853.	Familial testicular cancer: lack of evidence for trinucleotide repeat expansions and association with PKD1 in one family. [electronic resource] by Teh, B T Linblad, K Nord, B Kytölä, S Schalling, M Larsson, C Rapley, E Biggs, P Huddart, R Stratton, M Producer: 19990610 In: Journal of medical genetics vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	854.	Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus. [electronic resource] by Houdayer, C Lemonnier, A Gerard, M Chauve, C Tredano, M de Villemeur, T B Aymard, P Bonnefont, J P Feldmann, D Producer: 19990813 In: Clinical chemistry and laboratory medicine vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	855.	Efficacy of cascade testing for fragile X syndrome. [electronic resource] by Wildhagen, M F van Os, T A Polder, J J ten Kate, L P Habbema, J D Producer: 19990923 In: Journal of medical screening vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	856.	Preparation of human cDNas encoding expanded polyglutamine repeats. [electronic resource] by Peters, M F Ross, C A Producer: 19991216 In: Neuroscience letters vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	857.	Definition of the smallest pathological CAG expansion in SCA7. [electronic resource] by Nardacchione, A Orsi, L Brusco, A Franco, A Grosso, E Dragone, E Mortara, P Schiffer, D De Marchi, M Producer: 19991123 In: Clinical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	858.	Regional decrease in brain glucose metabolism in asymptomatic gene carriers of Machado-Joseph disease: a preliminary report. [electronic resource] by Soong, B W Liu, R S Producer: 19980507 In: Zhonghua yi xue za zhi = Chinese medical journal; Free China ed vol. 61 Availability: No items available. Save to lists Add to cart (remove)
	859.	Analysis of spinocerebellar ataxia type 2 in Gunma Prefecture in Japan: CAG trinucleotide expansion and clinical characteristics. [electronic resource] by Mizushima, K Watanabe, M Abe, K Aoki, M Itoyama, Y Shizuka, M Okamoto, K Shoji, M Producer: 19980827 In: Journal of the neurological sciences vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	860.	[Clinical and molecular genetic analyses of congenital myotonic dystrophy]. [electronic resource] by Kojo, T Arahata, K Producer: 19980324 In: Nihon rinsho. Japanese journal of clinical medicine vol. 55 Availability: No items available. Save to lists Add to cart (remove)

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