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	3601.	A rapid, reliable, and inexpensive method for detection of di- and trinucleotide repeat markers and disease loci from dried blood spots. [electronic resource] by Holden, J J Chalifoux, M Wing, M Julien-Inalsingh, C White, B N Producer: 19961213 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3602.	Severe mental retardation and macroorchidism without mutation in the FMR1 gene. [electronic resource] by Reyniers, E Wolff, G Tariverdian, G De Boulle, K Storm, K Kooy, R F Willems, P J Producer: 19961213 In: American journal of medical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3603.	Fragile X mental retardation protein: nucleocytoplasmic shuttling and association with somatodendritic ribosomes. [electronic resource] by Feng, Y Gutekunst, C A Eberhart, D E Yi, H Warren, S T Hersch, S M Producer: 19970326 In: The Journal of neuroscience : the official journal of the Society for Neuroscience vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	3604.	Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. [electronic resource] by Gunter, C Paradee, W Crawford, D C Meadows, K A Newman, J Kunst, C B Nelson, D L Schwartz, C Murray, A Macpherson, J N Sherman, S L Warren, S T Producer: 19981215 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3605.	Identification of a novel 45 repeat unstable allele associated with a disease phenotype at the MJD1/SCA3 locus. [electronic resource] by Padiath, Quasar Saleem Srivastava, Achal Kumar Roy, Sanghmitra Jain, Satish Brahmachari, Samir Kumar Producer: 20050314 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 133B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3606.	Unfolding of higher DNA structures formed by the d(CGG) triplet repeat by UP1 protein. [electronic resource] by Fukuda, Hirokazu Katahira, Masato Tanaka, Etsuko Enokizono, Yoshiaki Tsuchiya, Naoto Higuchi, Kumiko Nagao, Minako Nakagama, Hitoshi Producer: 20060104 In: Genes to cells : devoted to molecular & cellular mechanisms vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3607.	Neural progenitor cells from an adult patient with fragile X syndrome. [electronic resource] by Schwartz, Philip H Tassone, Flora Greco, Claudia M Nethercott, Hubert E Ziaeian, Boback Hagerman, Randi J Hagerman, Paul J Producer: 20050208 In: BMC medical genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3608.	Patterns of CAG repeat interruptions in SCA1 and SCA2 genes in relation to repeat instability. [electronic resource] by Sobczak, Krzysztof Krzyzosiak, Wlodzimierz J Producer: 20050310 In: Human mutation vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3609.	Neurophysiological study of facial chorea in patients with Huntington's disease. [electronic resource] by Muñoz, Esteban Cervera, Alvaro Valls-Solé, Josep Producer: 20030820 In: Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology vol. 114 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3610.	The AIB1 glutamine repeat polymorphism is not associated with risk of breast cancer before age 40 years in Australian women. [electronic resource] by Montgomery, Karen G Chang, Jiun-Horng Gertig, Dorota M Dite, Gillian S McCredie, Margaret R Giles, Graham G Southey, Melissa C Hopper, John L Campbell, Ian G Producer: 20060125 In: Breast cancer research : BCR vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3611.	Epithelio-mesenchymal transition in a neoplastic ovarian epithelial hybrid cell line. [electronic resource] by Maines-Bandiera, Sarah L Huntsman, David Lestou, Valia S Kuo, Wen-Lin Leung, Peter C K Horsman, R Douglas Wong, Alice S T Woo, Michelle M M Choi, Keith K C Roskelley, Calvin D Auersperg, Nelly Producer: 20050131 In: Differentiation; research in biological diversity vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3612.	Frailty, serum androgens, and the CAG repeat polymorphism: results from the Massachusetts Male Aging Study. [electronic resource] by Travison, Thomas G Shackelton, Rebecca Araujo, Andre B Morley, John E Williams, Rachel E Clark, Richard V McKinlay, John B Producer: 20100701 In: The Journal of clinical endocrinology and metabolism vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3613.	A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats. [electronic resource] by Boy, Jana Schmidt, Thorsten Schumann, Ulrike Grasshoff, Ute Unser, Samy Holzmann, Carsten Schmitt, Ina Karl, Tim Laccone, Franco Wolburg, Hartwig Ibrahim, Saleh Riess, Olaf Producer: 20100615 In: Neurobiology of disease vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3614.	Relationship between carnosinase gene CNDP1 leucine repeat polymorphism and the clinical outcome of Chinese PD patients. [electronic resource] by Poon, P Y-K Szeto, C-C Kwan, B C-H Chow, K-M Li, P K-T Producer: 20101221 In: Clinical nephrology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3615.	Decreased fragile X mental retardation protein (FMRP) is associated with lower IQ and earlier illness onset in patients with schizophrenia. [electronic resource] by Kovács, Tamás Kelemen, Oguz Kéri, Szabolcs Producer: 20150803 In: Psychiatry research vol. 210 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3616.	Aberrant splicing of HTT generates the pathogenic exon 1 protein in Huntington disease. [electronic resource] by Sathasivam, Kirupa Neueder, Andreas Gipson, Theresa A Landles, Christian Benjamin, Agnesska C Bondulich, Marie K Smith, Donna L Faull, Richard L M Roos, Raymund A C Howland, David Detloff, Peter J Housman, David E Bates, Gillian P Producer: 20130409 In: Proceedings of the National Academy of Sciences of the United States of America vol. 110 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3617.	Correlation of inter-locus polyglutamine toxicity with CAG•CTG triplet repeat expandability and flanking genomic DNA GC content. [electronic resource] by Nestor, Colm E Monckton, Darren G Producer: 20120720 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3618.	Androgen receptor polymorphisms and testicular cancer risk. [electronic resource] by Grassetti, D Giannandrea, F Paoli, D Masciandaro, P Figura, V Carlini, T Rizzo, F Lombardo, F Lenzi, A Gandini, L Producer: 20151230 In: Andrology vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3619.	Association of polymorphisms in the intron of [electronic resource] by Rao, Bhavna S Tharigopala, Arokiasamy Rachapalli, Sudhir R Rajagopal, Rama Soumittra, Nagasamy Producer: 20171218 In: Indian journal of ophthalmology vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3620.	Genetic load determines atrophy in hand cortico-striatal pathways in presymptomatic Huntington's disease. [electronic resource] by Hong, Yi O'Donnell, Lauren J Savadjiev, Peter Zhang, Fan Wassermann, Demian Pasternak, Ofer Johnson, Hans Paulsen, Jane Vonsattel, Jean-Paul Makris, Nikos Westin, Carl F Rathi, Yogesh Producer: 20190603 In: Human brain mapping vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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