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Results: 1-6 |
Results: 6

Authors: Reich, DE Cargill, M Bolk, S Ireland, J Sabeti, PC Richter, DJ Lavery, T Kouyoumjian, R Farhadian, SF Ward, R Lander, ES
Citation: De. Reich et al., Linkage disequilibrium in the human genome, NATURE, 411(6834), 2001, pp. 199-204

Authors: Altshuler, D Hirschhorn, JN Klannemark, M Lindgren, CM Vohl, MC Nemesh, J Lane, CR Schaffner, SF Bolk, S Brewer, C Tuomi, T Gaudet, D Hudson, TJ Daly, M Groop, L Lander, ES
Citation: D. Altshuler et al., The common PPAR gamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes, NAT GENET, 26(1), 2000, pp. 76-80

Authors: Hirschhorn, JN Sklar, P Lindblad-Toh, K Lim, YM Ruiz-Gutierrez, M Bolk, S Langhorst, B Schaffner, S Winchester, E Lander, ES
Citation: Jn. Hirschhorn et al., SBE-TAGS: An array-based method for efficient single-nucleotide polymorphism genotyping, P NAS US, 97(22), 2000, pp. 12164-12169

Authors: Bolk, S Pelet, A Hofstra, RMW Angrist, M Salomon, R Croaker, D Buys, CHCM Lyonnet, S Chakravarti, A
Citation: S. Bolk et al., A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus, P NAS US, 97(1), 2000, pp. 268-273

Authors: Bolk, S Puffenberger, EG Hudson, J Morton, DH Chakravarti, A
Citation: S. Bolk et al., Elevated frequency and allelic heterogeneity of congenital nephrotic syndrome, Finnish type, in the Old Order Mennonites, AM J HU GEN, 65(6), 1999, pp. 1785-1790

Authors: Angrist, M Bolk, S Bentley, K Nallasamy, S Halushka, MK Chakravarti, A
Citation: M. Angrist et al., Genomic structure of the gene for the SH2 and pleckstrin homology domain-containing protein GRB10 and evaluation of its role in Hirschsprung disease, ONCOGENE, 17(23), 1998, pp. 3065-3070
Risultati: 1-6 |