Your search returned 4032 results.

Results
	3161.	Alleles with short CAG and GGN repeats in the androgen receptor gene are associated with benign endometrial cancer. [electronic resource] by Rodríguez, Germán Bilbao, Cristina Ramírez, Raquel Falcón, Orlando León, Laureano Chirino, Ricardo Falcón, Orlando Díaz, B Pilar Rivero, Juan F Perucho, Manuel Díaz-Chico, B Nicolás Díaz-Chico, Juan C Producer: 20070529 In: International journal of cancer vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3162.	Low stability of Huntington muscle mitochondria against Ca2+ in R6/2 mice. [electronic resource] by Gizatullina, Zemfira Z Lindenberg, Katrin S Harjes, Phoebe Chen, Ying Kosinski, Christoph M Landwehrmeyer, Bernhard G Ludolph, Albert C Striggow, Frank Zierz, Stephan Gellerich, Frank N Producer: 20060425 In: Annals of neurology vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3163.	The guanine-rich fragile X chromosome repeats are reluctant to form tetraplexes. [electronic resource] by Fojtík, Petr Kejnovská, Iva Vorlícková, Michaela Producer: 20040121 In: Nucleic acids research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3164.	Concerted action of exonuclease and Gap-dependent endonuclease activities of FEN-1 contributes to the resolution of triplet repeat sequences (CTG)n- and (GAA)n-derived secondary structures formed during maturation of Okazaki fragments. [electronic resource] by Singh, Purnima Zheng, Li Chavez, Valerie Qiu, Junzhuan Shen, Binghui Producer: 20070323 In: The Journal of biological chemistry vol. 282 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3165.	Sequence variants within exon 1 of MECP2 occur in females with mental retardation. [electronic resource] by Harvey, Chris G Menon, Sailesh D Stachowiak, Beata Noor, Abdul Proctor, Adam Mensah, Albert K Mnatzakanian, Gevork N Alfred, Simon E Guo, Ray Scherer, Stephen W Kennedy, James L Roberts, Wendy Srivastava, Anand K Srivistava, Anand K Minassian, Berge A Vincent, John B Producer: 20070718 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 144B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3166.	Discrepancies in reporting the CAG repeat lengths for Huntington's disease. [electronic resource] by Quarrell, Oliver W Handley, Olivia O'Donovan, Kirsty Dumoulin, Christine Ramos-Arroyo, Maria Biunno, Ida Bauer, Peter Kline, Margaret Landwehrmeyer, G Bernhard Producer: 20120402 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3167.	The role of genetic and autoimmune factors in premature ovarian failure. [electronic resource] by Shamilova, Nigyar N Marchenko, Larisa A Dolgushina, Nataliya V Zaletaev, Dmitry V Sukhikh, Gennady T Producer: 20131113 In: Journal of assisted reproduction and genetics vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3168.	Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls. [electronic resource] by Jiang, H Sun, Y M Hao, Y Yan, Y P Chen, K Xin, S H Tang, Y P Li, X H Jun, T Chen, Y Y Liu, Z J Wang, C R Li, H Pei, Z Shang, H F Zhang, B R Gu, W H Wu, Z Y Tang, B S Burgunder, J-M Producer: 20141106 In: European journal of neurology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3169.	Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification. [electronic resource] by De Antonio, M Dogan, C Hamroun, D Mati, M Zerrouki, S Eymard, B Katsahian, S Bassez, G Producer: 20170411 In: Revue neurologique vol. 172 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3170.	Phenobarbital use and neurological problems in FMR1 premutation carriers. [electronic resource] by Saldarriaga, Wilmar Lein, Pamela González Teshima, Laura Yuriko Isaza, Carolina Rosa, Lina Polyak, Andrew Hagerman, Randi Girirajan, Santhosh Silva, Marisol Tassone, Flora Producer: 20161219 In: Neurotoxicology vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3171.	The Saccharomyces cerevisiae Mre11-Rad50-Xrs2 complex promotes trinucleotide repeat expansions independently of homologous recombination. [electronic resource] by Ye, Yanfang Kirkham-McCarthy, Lucy Lahue, Robert S Producer: 20170515 In: DNA repair vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3172.	Oxidized dNTPs and the OGG1 and MUTYH DNA glycosylases combine to induce CAG/CTG repeat instability. [electronic resource] by Cilli, Piera Ventura, Ilenia Minoprio, Anna Meccia, Ettore Martire, Alberto Wilson, Samuel H Bignami, Margherita Mazzei, Filomena Producer: 20170526 In: Nucleic acids research vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3173.	A modifier of Huntington's disease onset at the MLH1 locus. [electronic resource] by Lee, Jong-Min Chao, Michael J Harold, Denise Abu Elneel, Kawther Gillis, Tammy Holmans, Peter Jones, Lesley Orth, Michael Myers, Richard H Kwak, Seung Wheeler, Vanessa C MacDonald, Marcy E Gusella, James F Producer: 20180123 In: Human molecular genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3174.	Simple sequence repeats for germplasm analysis and mapping in maize. [electronic resource] by Taramino, G Tingey, S Producer: 19970108 In: Genome vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3175.	Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene. [electronic resource] by Milà, M Castellví-Bel, S Sánchez, A Lázaro, C Villa, M Estivill, X Producer: 19960925 In: Journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3176.	A reproducible assay of polymerase chain reaction to detect trinucleotide repeat expansion of Huntington's disease and senile chorea. [electronic resource] by Watanabe, M Abe, K Aoki, M Kameya, T Itoyama, Y Shoji, M Ikeda, M Iizuka, T Hirai, S Producer: 19961009 In: Neurological research vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3177.	New findings in the behavioral profile of young FraX females. [electronic resource] by Borghgraef, M Umans, S Steyaert, J Legius, E Fryns, J P 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)
	3178.	A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion. [electronic resource] by Milà, M Castellví-Bel, S Giné, R Vazquez, C Badenas, C Sánchez, A Estivill, X Producer: 19961015 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3179.	A Huntington disease-like neurodegenerative disorder maps to chromosome 20p. [electronic resource] by Xiang, F Almqvist, E W Huq, M Lundin, A Hayden, M R Edström, L Anvret, M Zhang, Z Producer: 19981223 In: American journal of human genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3180.	Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodies. [electronic resource] by Tam, Mandy Erin Montgomery, S Kekis, Mariana Stollar, B David Price, Gerald B Pearson, Christopher E Producer: 20031021 In: Journal of molecular biology vol. 332 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

Refine your search

Availability

Authors

Topics

Languages

Your search returned 4032 results.