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Results 1-10 of 20 (Search time: 0.002 seconds).
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First PublishedTitleAuthor(s)Type
1-Jun-2014A major recombination hotspot in the XqYq pseudoautosomal region gives new insight into processing of human gene conversion eventsSarbajna, Shriparna; Denniff, Matthew; Jeffreys, Alec J.; Neumann, Rita; Artigas, María Soler; Veselis, Amelia; May, Celia A.Journal Article
Nov-2008Identifying genetic traces of historical expansions: Phoenician footprints in the Mediterranean.Zalloua, PA; Platt, DE; El Sibai M; Khalife, J; Makhoul, N; Haber, M; Xue, Y; Izaabel, H; Bosch, E; Adams, SM; Arroyo, E; López-Parra, AM; Aler, M; Picornell, A; Ramon, M; Jobling, MA; Comas, D; Bertranpetit, J; Wells, RS; Tyler-Smith, C; Genographic, ConsortiumJournal Article
1-Sep-2009Genetic diversity and the emergence of ethnic groups in Central Asia.Heyer, E.; Balaresque, Patricia; Jobling, Mark A.; Quintana-Murci, L.; Chaix, R.; Segurel, L.; Aldashev, A.; Hegay, T.Journal Article
Nov-2004Y chromosome haplogroups of elite Ethiopian endurance runners.Moran, CN; Scott, RA; Adams, SM; Warrington, SJ; Jobling, MA; Wilson, RH; Goodwin, WH; Georgiades, E; Wolde, B; Pitsiladis, YPJournal Article
Apr-2003High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysis.Bosch, E; Calafell, F; Rosser, ZH; Nørby, S; Lynnerup, N; Hurles, ME; Jobling, MAJournal Article
Mar-2006Estimating sex-specific processes in human populations: Are XY-homologous markers an effective tool?Balaresque, P; Manni, F; Dugoujon, JM; Crousau-Roy, B; Heyer, EJournal Article
Nov-2006Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.Tarpey, P; Thomas, S; Sarvananthan, N; Mallya, U; Lisgo, S; Talbot, CJ; Roberts, EO; Awan, M; Surendran, M; McLean, RJ; Reinecke, RD; Langmann, A; Lindner, S; Koch, M; Jain, S; Woodruff, G; Gale, RP; Bastawrous, A; Degg, C; Droutsas, K; Asproudis, I; Zubcov, AA; Pieh, C; Veal, CD; Machado, RD; Backhouse, OC; Baumber, L; Constantinescu, CS; Brodsky, MC; Hunter, DG; Hertle, RW; Read, RJ; Edkins, S; O'Meara, S; Parker, A; Stevens, C; Teague, J; Wooster, R; Futreal, PA; Trembath, RC; Stratton, MR; Raymond, FL; Gottlob, IJournal Article
Oct-2005Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level.Barber, JC; Maloney, V; Hollox, EJ; Stuke-Sontheimer, A; du Bois G; Daumiller, E; Klein-Vogler, U; Dufke, A; Armour, JA; Liehr, TJournal Article
Dec-2004Molecular evidence for absence of Y-linkage of the Hairy Ears trait.Lee, AC; Kamalam, A; Adams, SM; Jobling, MAJournal Article
10-Aug-200626-Locus Y-STR typing in a Bhutanese population sample.Parkin, EJ; Kraayenbrink, T; van Driem GL; Tshering Of Gaselô K; de Knijff P; Jobling, MAJournal Article