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	31301.	Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY. [electronic resource] by Chen, C P Chern, S R Chang, C L Lee, C C Chen, W L Chen, L F Wang, W Producer: 20001025 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31302.	The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. I. An autosomal genome scan for genes that predispose to type 2 diabetes. [electronic resource] by Ghosh, S Watanabe, R M Valle, T T Hauser, E R Magnuson, V L Langefeld, C D Ally, D S Mohlke, K L Silander, K Kohtamäki, K Chines, P Balow, J Birznieks, G Chang, J Eldridge, W Erdos, M R Karanjawala, Z E Knapp, J I Kudelko, K Martin, C Morales-Mena, A Musick, A Musick, T Pfahl, C Porter, R Rayman, J B Producer: 20001214 In: American journal of human genetics vol. 67 Availability: No items available. Save to lists Add to cart (remove)
	31303.	NRL S50T mutation and the importance of 'founder effects' in inherited retinal dystrophies. [electronic resource] by Bessant, D A Payne, A M Plant, C Bird, A C Swaroop, A Bhattacharya, S S Producer: 20010201 In: European journal of human genetics : EJHG vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31304.	Large deletions at the t(9;22) breakpoint are common and may identify a poor-prognosis subgroup of patients with chronic myeloid leukemia. [electronic resource] by Sinclair, P B Nacheva, E P Leversha, M Telford, N Chang, J Reid, A Bench, A Champion, K Huntly, B Green, A R Producer: 20000224 In: Blood vol. 95 Availability: No items available. Save to lists Add to cart (remove)
	31305.	Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS. [electronic resource] by Blau, N Scherer-Oppliger, T Baumer, A Riegel, M Matasovic, A Schinzel, A Jaeken, J Thöny, B Producer: 20000822 In: Human mutation vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31306.	Papillary urothelial hyperplasia is a clonal precursor to papillary transitional cell bladder cancer. [electronic resource] by Chow, N H Cairns, P Eisenberger, C F Schoenberg, M P Taylor, D C Epstein, J I Sidransky, D Producer: 20001222 In: International journal of cancer vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	31307.	AP-1 mediated relief of repressive activity of the CD30 promoter microsatellite in Hodgkin and Reed-Sternberg cells. [electronic resource] by Watanabe, Mariko Ogawa, Yuji Ito, Kinji Higashihara, Masaaki Kadin, Marshall E Abraham, Lawrence J Watanabe, Toshiki Horie, Ryouichi Producer: 20030910 In: The American journal of pathology vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31308.	HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. [electronic resource] by Howell, V M Haven, C J Kahnoski, K Khoo, S K Petillo, D Chen, J Fleuren, G J Robinson, B G Delbridge, L W Philips, J Nelson, A E Krause, U Hammje, K Dralle, H Hoang-Vu, C Gimm, O Marsh, D J Morreau, H Teh, B T Producer: 20030930 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31309.	Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect. [electronic resource] by Bachinski, Linda L Udd, Bjarne Meola, Giovanni Sansone, Valeria Bassez, Guillaume Eymard, Bruno Thornton, Charles A Moxley, Richard T Harper, Peter S Rogers, Mark T Jurkat-Rott, Karin Lehmann-Horn, Frank Wieser, Thomas Gamez, Josep Navarro, Carmen Bottani, Armand Kohler, Andre Shriver, Mark D Sallinen, Riitta Wessman, Maija Zhang, Shanxiang Wright, Fred A Krahe, Ralf Producer: 20031121 In: American journal of human genetics vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31310.	Genome wide scan using homozygosity mapping and linkage analyses of a single pedigree with affective disorder suggests oligogenic inheritance. [electronic resource] by Ewald, Henrik Kruse, Torben A Mors, Ole Producer: 20040219 In: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics vol. 120B Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31311.	Linkage analysis of candidate loci for end-stage renal disease due to diabetic nephropathy. [electronic resource] by Iyengar, Sudha K Fox, Katherine A Schachere, Marlene Manzoor, Fauzia Slaughter, Mary E Covic, Adrian M Orloff, S Mohammed Hayden, Patrick S Olson, Jane M Schelling, Jeffrey R Sedor, John R Producer: 20030814 In: Journal of the American Society of Nephrology : JASN vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31312.	Combined 17alpha-Hydroxylase/17,20-lyase deficiency caused by Phe93Cys mutation in the CYP17 gene. [electronic resource] by Di Cerbo, Alfredo Biason-Lauber, Anna Savino, Maria Piemontese, Maria Rosaria Di Giorgio, Anna Perona, Marco Savoia, Anna Producer: 20020301 In: The Journal of clinical endocrinology and metabolism vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31313.	Somatic mutations of the lysyl oxidase gene on chromosome 5q23.1 in colorectal tumors. [electronic resource] by Csiszar, Katalin Fong, Sheri F T Ujfalusi, Aniko Krawetz, Stephen A Salvati, Eugene P Mackenzie, James W Boyd, Charles D Producer: 20020208 In: International journal of cancer vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31314.	Genetic susceptibility to fibrocalculous pancreatic diabetes in Bangladeshi subjects: a family study. [electronic resource] by Chowdhury, Z Md McDermott, M F Davey, S Hassan, Z Sinnott, P J Hemmatpour, S K Sherwin, S Ali, L Aganna, E Allotey, R A North, B V Cassell, P G Azad Khan, A K Hitman, G A Producer: 20020614 In: Genes and immunity vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31315.	[Microsatellite alterations on chromosome 9p21-22 in sporadic colorectal cancer]. [electronic resource] by Zhang, Y Lai, M Producer: 20030613 In: Zhonghua bing li xue za zhi = Chinese journal of pathology vol. 28 Availability: No items available. Save to lists Add to cart (remove)
	31316.	Detection of universal variable fragments as markers for genetic studies. A novel technology for DNA fingerprinting. [electronic resource] by van Haeringen, W A van de Goor, L H P Panneman, H van Lith, H A van Haeringen, H van Zutphen, L F M Producer: 20030910 In: Molecular biotechnology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31317.	A meta-analysis of whole genome linkage screens in multiple sclerosis. [electronic resource] Producer: 20040212 In: Journal of neuroimmunology vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31318.	Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHIT. [electronic resource] by Larson, Garry P Ding, Yan Cheng, Li S-C Lundberg, Cathryn Gagalang, Virgil Rivas, Guillermo Geller, Louis Weitzel, Jeffrey MacDonald, Deborah Archambeau, John Slater, Jerry Neuberg, Donna Daly, Mary B Angel, Irene Benson, Al B Smith, Kimberly Kirkwood, John M O'Dwyer, Peter J Raskay, Barbara Sutphen, Rebecca Drew, Rosalind Stewart, James A Werndli, Jae Johnson, David Ruckdeschel, John C Elston, Robert C Krontiris, Theodore G Producer: 20050314 In: Cancer research vol. 65 Availability: No items available. Save to lists Add to cart (remove)
	31319.	Lack of association between polymorphic microsatellites of the VMAT2 gene and Parkinson's disease in Japan. [electronic resource] by Kariya, Shingo Hirano, Makito Takahashi, Nobuyuki Furiya, Yoshiko Ueno, Satoshi Producer: 20050721 In: Journal of the neurological sciences vol. 232 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31320.	Association between Toll-like receptor 4 and inflammatory bowel disease. [electronic resource] by Oostenbrug, Liekele E Drenth, Joost P H de Jong, Dirk J Nolte, Ilja M Oosterom, Elvira van Dullemen, Hendrik M van der Linde, Klaas te Meerman, Gerard J van der Steege, Gerrit Kleibeuker, Jan H Jansen, Peter L M Producer: 20050830 In: Inflammatory bowel diseases vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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