Search

Microsatellite repeats
 
Advanced search
Browse by...
Refine your research by the most used items
Deposit
Highlights
More informations
Show items per page
Elements: 26
Page 1 on 2
 TitleAuthors / EditorsDate
add to browser selection
 What is expanded in progressive myoclonus epilepsy? Lalioti, M. D.; Scott, Hamish Steele; Antonarakis, Stylianos 1997
add to browser selection
 PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy Guicheney, P; Vignier, N; Zhang, X; He, Y; ... Tryggvason, K 1998
add to browser selection
 Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 Blouin, Jean-Louis; Dombroski, B. A.; Nath, S. K.; Lasseter, V. K.; ... Pulver, A. E. 1998
add to browser selection
 Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer Bapat, B V; Madlensky, L; Temple, L K; Hiruki, T; ... Gallinger, S 1999
add to browser selection
 The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster Neerman Arbez, Marguerite; Antonarakis, Stylianos; Honsberger, A.; Morris, Michael Andréw 1999
add to browser selection
 Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B Wiszniewski, W.; Fondaneche, M. C.; Lambert, N.; Masternak, Krzysztof; ... Lisowska-Grospierre, B. 2000
add to browser selection
 Genome search for susceptibility loci of common idiopathic generalised epilepsies Sander, T; Schulz, H; Saar, K; Gennaro, E; ... Reis, A 2000
add to browser selection
 Enhanced susceptibility to lupus contributed from the nonautoimmune C57BL/10, but not C57BL/6, genome Rozzo, S. J.; Vyse, T. J.; Menze, K.; Izui, Shozo; Kotzin, B. L. 2000
add to browser selection
 Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity Blouin, Jean-Louis; Meeks, M.; Radhakrishna, U.; Sainsbury, A.; ... Antonarakis, Stylianos 2000
add to browser selection
 An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos 2001
add to browser selection
 Comparison of microsatellite instability and chromosomal instability in predicting survival of patients with T3N0 colorectal cancer Gervaz, Pascal; Cerottini, Jean-Philippe; Bouzourene, Hanifa; Hahnloser, Dieter; ... Carethers, John M 2002
add to browser selection
 Prospective evaluation of genetic abnormalities and telomerase expression in exfoliated urinary cells for bladder cancer detection Neves, Manuel; Ciofu, Calin; Larousserie, Frederique; Fleury, Jocelyne; ... Gattegno, Bernard 2002
add to browser selection
 Differential rates of frameshift alterations in four repeat sequences of hereditary nonpolyposis colorectal cancer tumors Giacobino, Ariane; Rey-Berthod, Claudine; Couturier, Alexia; Antonarakis, Stylianos; Hutter, Pierre 2002
add to browser selection
 Prostate cancer is part of the hereditary non-polyposis colorectal cancer (HNPCC) tumor spectrum Soravia, Claudio; van der Klift, Heleen; Brundler, Marie-Anne; Blouin, Jean-Louis; ... Delozier-Blanchet, Célia 2003
add to browser selection
 A new DR7-DQ8 haplotype resulting from a recombination between the DQA1 and DQB1 loci in a leukemic patient of Caucasoid origin Tiercy, Jean-Marie; Villard, Jean 2004
add to browser selection
 Two colons-two cancers: paradigm shift and clinical implications Gervaz, Pascal; Bucher, Pascal Alain Robert; Morel, Philippe 2004
add to browser selection
 De novo concurrent papillary renal cell carcinoma and angiomyolipoma in a kidney allograft: evidence of donor origin Rotman, Samuel; Deruaz, Cédric; Venetz, Jean-Pierre; Chaubert, Pascal; ... Lemoine, Robert 2006
add to browser selection
 Influence of target gene mutations on survival, stage and histology in sporadic microsatellite unstable colon cancers Jung, Barbara; Smith, E Julieta; Doctolero, Ryan T; Gervaz, Pascal; ... Carethers, John M 2006
add to browser selection
 Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of events Dahoun, Sophie; Gagos, Sarantis; Gagnebin, Maryline; Gehrig, Corinne; ... Blouin, Jean-Louis 2008
add to browser selection
 HLA-B51 and haplotypic diversity of B-Cw associations: implications for matching in unrelated hematopoietic stem cell transplantation Bettens, F.; Nicoloso de Faveri, G.; Tiercy, Jean-Marie 2009
<< previous | 1 | 2 |