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	1821.	Factors related to genetic testing in adults at risk for Huntington disease: the prospective Huntington at-risk observational study (PHAROS). [electronic resource] by Quaid, K A Eberly, S W Kayson-Rubin, E Oakes, D Shoulson, I Producer: 20180109 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1822.	Tremor-Ataxia syndrome and primary ovarian insufficiency in an [electronic resource] by Saldarriaga-Gil, Wilmar Rodriguez-Guerrero, Tatiana Fandiño-Losada, Andres Ramirez-Cheyne, Julian Producer: 20180803 In: Colombia medica (Cali, Colombia) vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1823.	Measuring Dynamic Behavior of Trinucleotide Repeat Tracts In Vivo in Saccharomyces cerevisiae. [electronic resource] by Williams, Gregory M Surtees, Jennifer A Producer: 20180606 In: Methods in molecular biology (Clifton, N.J.) vol. 1672 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1824.	Delayed Onset and Reduced Cognitive Deficits through Pre-Conditioning with 3-Nitropropionic Acid is Dependent on Sex and CAG Repeat Length in the R6/2 Mouse Model of Huntington's Disease. [electronic resource] by Skillings, Elizabeth A Morton, A Jennifer Producer: 20161216 In: Journal of Huntington's disease vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1825.	Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation. [electronic resource] by Sen, Nesli-Ece Canet-Pons, Júlia Halbach, Melanie V Arsovic, Aleksandar Pilatus, Ulrich Chae, Woon-Hyung Kaya, Zeynep-Ece Seidel, Kay Rollmann, Ewa Mittelbronn, Michel Meierhofer, David De Zeeuw, Chris I Bosman, Laurens W J Gispert, Suzana Auburger, Georg Producer: 20200727 In: Neurobiology of disease vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1826.	Comparison of NGS panel and Sanger sequencing for genotyping CAG repeats in the AR gene. [electronic resource] by Rocca, Maria Santa Ferrarini, Margherita Msaki, Aichi Vinanzi, Cinzia Ghezzi, Marco De Rocco Ponce, Maurizio Foresta, Carlo Ferlin, Alberto Producer: 20210413 In: Molecular genetics & genomic medicine vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1827.	Identification of two nuclear proteins which bind to RNA CUG repeats: significance for myotonic dystrophy. [electronic resource] by Bhagavati, S Bhagwati, S Ghatpande, A Leung, B Producer: 19961213 In: Biochemical and biophysical research communications vol. 228 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1828.	The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy. [electronic resource] by Sander, T Peters, C Janz, D Bianchi, A Bauer, G Wienker, T F Hildmann, T Epplen, J T Riess, O Producer: 19980416 In: Epilepsy research vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1829.	Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes? [electronic resource] by Schöls, L Amoiridis, G Büttner, T Przuntek, H Epplen, J T Riess, O Producer: 19980102 In: Annals of neurology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1830.	Bioenergetics in Huntington's disease. [electronic resource] by Grünewald, T Beal, M F Producer: 20000225 In: Annals of the New York Academy of Sciences vol. 893 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1831.	A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation. [electronic resource] by Huggins, R M Loesch, D Z Sherman, S L Producer: 19990413 In: Annals of human genetics vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1832.	Therapeutic opportunities in polyglutamine disease. [electronic resource] by Hughes, R E Olson, J M Producer: 20010426 In: Nature medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1833.	Frequency analysis of autosomal dominant cerebellar ataxias in Taiwanese patients and clinical and molecular characterization of spinocerebellar ataxia type 6. [electronic resource] by Soong B, W Lu Y, C Choo K, B Lee H, Y Producer: 20010802 In: Archives of neurology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1834.	[Prevention of fragile X syndrome by prenatal genetic diagnosis: advantages and controversial aspects]. [electronic resource] by Tejada, M I Producer: 20041102 In: Revista de neurologia vol. 33 Suppl 1 Availability: No items available. Save to lists Add to cart (remove)
	1835.	Two novel single-base-pair substitutions adjacent to the CAG repeat in the huntington disease gene (IT15): implications for diagnostic testing. [electronic resource] by Margolis, R L Stine, O C Callahan, C Rosenblatt, A Abbott, M H Sherr, M Ross, C A Producer: 19990310 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1836.	Identification of the spinocerebellar ataxia type 7 mutation in Taiwan: application of PCR-based Southern blot. [electronic resource] by Hsieh, M Lin, S J Chen, J F Lin, H M Hsiao, K M Li, S Y Li, C Tsai, C J Producer: 20010201 In: Journal of neurology vol. 247 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1837.	Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12. [electronic resource] by Holmes, S E O'Hearn, E E McInnis, M G Gorelick-Feldman, D A Kleiderlein, J J Callahan, C Kwak, N G Ingersoll-Ashworth, R G Sherr, M Sumner, A J Sharp, A H Ananth, U Seltzer, W K Boss, M A Vieria-Saecker, A M Epplen, J T Riess, O Ross, C A Margolis, R L Producer: 19991220 In: Nature genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1838.	Late onset levodopa responsive Huntington's disease with minimal chorea masquerading as Parkinson plus syndrome. [electronic resource] by Reuter, I Hu, M T Andrews, T C Brooks, D J Clough, C Chaudhuri, K R Producer: 20000301 In: Journal of neurology, neurosurgery, and psychiatry vol. 68 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1839.	GAA expansion size and age at onset of Friedreich's ataxia. [electronic resource] by Mateo, I Llorca, J Volpini, V Corral, J Berciano, J Combarros, O Producer: 20040427 In: Neurology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	1840.	Androgen receptor gene GGN repeat length and reproductive characteristics in young Swedish men. [electronic resource] by Lundin, K B Giwercman, Y L Rylander, L Hagmar, L Giwercman, A Producer: 20060927 In: European journal of endocrinology vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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