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	3001.	Microdeletions in FMR2 may be a significant cause of premature ovarian failure. [electronic resource] by Murray, A Webb, J Dennis, N Conway, G Morton, N Producer: 19991119 In: Journal of medical genetics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3002.	[The function of Huntington disease gene product (huntingtin) and the pathomechanism of Huntington disease]. [electronic resource] by Nukina, N Producer: 19990601 In: Nihon rinsho. Japanese journal of clinical medicine vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	3003.	Polymorphic repeats in the androgen receptor gene in high-risk sibships. [electronic resource] by Miller, E A Stanford, J L Hsu, L Noonan, E Ostrander, E A Producer: 20010830 In: The Prostate vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3004.	Racial variation in CAG repeat lengths within the androgen receptor gene among prostate cancer patients of lower socioeconomic status. [electronic resource] by Bennett, Charles L Price, Douglas K Kim, Simon Liu, Dachao Jovanovic, Borko D Nathan, Derek Johnson, Margaret E Montgomery, Jeffrey S Cude, Kelly Brockbank, Justin C Sartor, Oliver Figg, William D Producer: 20020918 In: Journal of clinical oncology : official journal of the American Society of Clinical Oncology vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3005.	Analysis of G/A polymorphism in the androgen response element I of the PSA gene and its interactions with the androgen receptor polymorphisms. [electronic resource] by Rao, Anuradha Chang, Bao-L i Hawkins, Gregory Hu, Jennifer J Rosser, Charles J Hall, M Craig Meyers, Deborah A Xu, Jianfeng Cramer, Scott D Producer: 20030807 In: Urology vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3006.	Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation. [electronic resource] by Hagerman, R J Leavitt, B R Farzin, F Jacquemont, S Greco, C M Brunberg, J A Tassone, F Hessl, D Harris, S W Zhang, L Jardini, T Gane, L W Ferranti, J Ruiz, L Leehey, M A Grigsby, J Hagerman, P J Producer: 20040603 In: American journal of human genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3007.	Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. [electronic resource] by Lloret, Alejandro Dragileva, Ella Teed, Allison Espinola, Janice Fossale, Elisa Gillis, Tammy Lopez, Edith Myers, Richard H MacDonald, Marcy E Wheeler, Vanessa C Producer: 20060810 In: Human molecular genetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3008.	Medicine. Anticipating trouble from gene transcription. [electronic resource] by Fortini, Mark E Producer: 20070412 In: Science (New York, N.Y.) vol. 315 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3009.	Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene. [electronic resource] by Musova, Zuzana Mazanec, Radim Krepelova, Anna Ehler, Edvard Vales, Jiri Jaklova, Radka Prochazka, Tomas Koukal, Petr Marikova, Tatana Kraus, Josef Havlovicova, Marketa Sedlacek, Zdenek Producer: 20090923 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3010.	CGG trinucleotide repeat length modulates neural plasticity and spatiotemporal processing in a mouse model of the fragile X premutation. [electronic resource] by Hunsaker, Michael R Kim, Kyoungmi Willemsen, Rob Berman, Robert F Producer: 20130627 In: Hippocampus vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3011.	The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease. [electronic resource] by Klempíř, Jiří Zidovská, Jana Stochl, Jan Ing, Věra Kebrdlová Uhrová, Tereza Roth, Jan Producer: 20110606 In: Movement disorders : official journal of the Movement Disorder Society vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3012.	[Triplet repeat disease, with particular emphasis of spinal and bulbar muscular atrophy (SBMA)]. [electronic resource] by Sobue, G Producer: 20010927 In: Rinsho shinkeigaku = Clinical neurology vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	3013.	[Proximal weakness and exercise-induced pain as initial symptom of oculopharyngeal muscular dystrophy]. [electronic resource] by Lampe, J B Schäfer, J Gärtner, H J Reichmann, H Producer: 20020103 In: Der Nervenarzt vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3014.	Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue specificity, but no association with cell division rates. [electronic resource] by Gomes-Pereira, M Fortune, M T Monckton, D G Producer: 20010705 In: Human molecular genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3015.	Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. [electronic resource] by Miller, J W Urbinati, C R Teng-Umnuay, P Stenberg, M G Byrne, B J Thornton, C A Swanson, M S Producer: 20001024 In: The EMBO journal vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3016.	Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2. [electronic resource] by Horwitz, M Benson, K F Li, F Q Wolff, J Leppert, M F Hobson, L Mangelsdorf, M Yu, S Hewett, D Richards, R I Raskind, W H Producer: 19971107 In: American journal of human genetics vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3017.	[Analyses of dominant mutations and their phenotypes: unraveling of physiological functions of retinoid and identification of the responsible gene for Machado-Joseph disease]. [electronic resource] by Kakizuka, A Producer: 19970514 In: Seikagaku. The Journal of Japanese Biochemical Society vol. 69 Availability: No items available. Save to lists Add to cart (remove)
	3018.	Genomic features of human PKR: alternative splicing and a polymorphic CGG repeat in the 5'-untranslated region. [electronic resource] by Xu, Z Williams, B R Producer: 19981119 In: Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3019.	Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's ataxia. [electronic resource] by De Michele, G Cavalcanti, F Criscuolo, C Pianese, L Monticelli, A Filla, A Cocozza, S 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)
	3020.	CAG repeat polymorphism within the KCNN3 gene is a significant contributor to susceptibility to anorexia nervosa: a case-control study of female patients and several ethnic groups in the Israeli Jewish population. [electronic resource] by Koronyo-Hamaoui, Maya Gak, Eva Stein, Daniel Frisch, Amos Danziger, Yardena Leor, Shani Michaelovsky, Elena Laufer, Neil Carel, Cynthia Fennig, Silvana Mimouni, Marc Apter, Alan Goldman, Boleslav Barkai, Gad Weizman, Abraham Producer: 20050208 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 131B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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