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	3261.	Analysis of triplet repeats in the huntingtin gene in Japanese families affected with Huntington's disease. [electronic resource] by Masuda, N Goto, J Murayama, N Watanabe, M Kondo, I Kanazawa, I Producer: 19960213 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3262.	Palindrome resolution and recombination in the mammalian germ line. [electronic resource] by Akgün, E Zahn, J Baumes, S Brown, G Liang, F Romanienko, P J Lewis, S Jasin, M Producer: 19970922 In: Molecular and cellular biology vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3263.	Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon. [electronic resource] by Annane, D Fiorelli, M Mazoyer, B Pappata, S Eymard, B Radvanyi, H Junien, C Fardeau, M Merlet, P Gajdos, P Syrota, A Sansom, Y Duboc, D Producer: 19980608 In: Neuromuscular disorders : NMD vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3264.	Fragile X DNA triplet repeats, (GCC)n, form hairpins with single hydrogen-bonded cytosine.cytosine mispairs at the CpG sites: isotope-edited nuclear magnetic resonance spectroscopy on (GCC)n with selective 15N4-labeled cytosine bases. [electronic resource] by Mariappan, S V Silks, L A Bradbury, E M Gupta, G Producer: 19981105 In: Journal of molecular biology vol. 283 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3265.	A simple method for the detection of neurologic disorders associated with CAG repeat expansion using PCR-microtiter plate hybridization. [electronic resource] by Lee, Y Oh, M R Kim, C H Hwang, H Z Kim, J S Song, S M Jin, D K Producer: 20020712 In: Journal of biotechnology vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3266.	Transcription and nuclear transport of CAG/CTG trinucleotide repeats in yeast. [electronic resource] by Fabre, Emmanuelle Dujon, Bernard Richard, Guy-Franck Producer: 20020930 In: Nucleic acids research vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3267.	[Eugonadotropic germinal cell failure (idiopathic germinal cell failure)]. [electronic resource] by Fukabori, Yoshitatsu Yoshida, Ken-ichiro Producer: 20060912 In: Nihon rinsho. Japanese journal of clinical medicine vol. Suppl 2 Availability: No items available. Save to lists Add to cart (remove)
	3268.	Androgen receptor gene exon 1 CAG repeat polymorphism in Finnish patients with childhood-onset type 1 diabetes. [electronic resource] by Gombos, Zsofia Hermann, Robert Veijola, Riitta Knip, Mikael Simell, Olli Pöllänen, Pasi Ilonen, Jorma Producer: 20040205 In: European journal of endocrinology vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3269.	Frequency and coverage of trinucleotide repeats in eukaryotes. [electronic resource] by Astolfi, Paola Bellizzi, Dina Sgaramella, Vittorio Producer: 20040122 In: Gene vol. 317 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3270.	Sharing of polyglutamine localization by the neuronal nucleus and cytoplasm in CAG-repeat diseases. [electronic resource] by Yamada, M Tan, C-F Inenaga, C Tsuji, S Takahashi, H Producer: 20050113 In: Neuropathology and applied neurobiology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3271.	Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17. [electronic resource] by Oda, Masaya Maruyama, Hirofumi Komure, Osamu Morino, Hiroyuki Terasawa, Hideo Izumi, Yuishin Imamura, Tohru Yasuda, Minoru Ichikawa, Keiji Ogawa, Masafumi Matsumoto, Masayasu Kawakami, Hideshi Producer: 20040308 In: Archives of neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3272.	Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review. [electronic resource] by Wardle, Mark Morris, Huw R Robertson, Neil P Producer: 20100115 In: Movement disorders : official journal of the Movement Disorder Society vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3273.	Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7). [electronic resource] by Hugosson, Therése Gränse, Lotta Ponjavic, Vesna Andréasson, Sten Producer: 20090311 In: Ophthalmic genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3274.	Genetic analysis of reelin gene (RELN) SNPs: no association with autism spectrum disorder in the Indian population. [electronic resource] by Dutta, Shruti Sinha, Swagata Ghosh, Saurabh Chatterjee, Anindita Ahmed, Shabina Usha, Rajamma Producer: 20081105 In: Neuroscience letters vol. 441 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3275.	Microsatellite marker development for the rubber tree (Hevea brasiliensis): characterization and cross-amplification in wild Hevea species. [electronic resource] by Mantello, Camila C Suzuki, Fernando I Souza, Livia M Gonçalves, Paulo S Souza, Anete P Producer: 20130131 In: BMC research notes vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3276.	Fat-free mass and its predictors in Huntington's disease. [electronic resource] by Süssmuth, S D Müller, V M Geitner, C Landwehrmeyer, G B Iff, S Gemperli, A Orth, Michael Producer: 20160309 In: Journal of neurology vol. 262 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3277.	Evaluation of parkinsonism and striatal dopamine transporter loss in patients with spinocerebellar ataxia type 6. [electronic resource] by Xie, Tao Appelbaum, Daniel Bernard, Jacqueline Padmanaban, Mahesh Pu, Yonglin Gomez, Christopher Producer: 20170407 In: Journal of neurology vol. 263 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3278.	Baseline Variables Associated with Functional Decline in 2CARE, A Randomized Clinical Trial in Huntington's Disease. [electronic resource] by McGarry, Andrew McDermott, Michael P Kieburtz, Karl Peng, Jing Cudkowicz, Merit Producer: 20210407 In: Journal of Huntington's disease vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3279.	The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeat. [electronic resource] by Steinbach, P Gläser, D Vogel, W Wolf, M Schwemmle, S Producer: 19980406 In: American journal of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3280.	Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy. [electronic resource] by Winchester, C L Ferrier, R K Sermoni, A Clark, B J Johnson, K J Producer: 19990503 In: Human molecular 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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