Zobrazeno 1 - 10
of 60
pro vyhledávání: '"L. R. Weitkamp"'
Publikováno v:
Animal Genetics. 19:317-330
The transmission ratios of alleles at 12 protein marker loci were computed individually for American Standardbred stallions in a genealogy of 5392 phenotyped horses. Over all loci there was significant gene transmission distortion for trotting stalli
Autor:
L. R. Weitkamp
Publikováno v:
Tissue Antigens. 7:273-279
Further data on the linkage relationships of red cell glyoxalase I(GLO) with HLA and Bf are reported. The most likely order of loci is GLO: Bf: HLA-B: HLA-A. No sex difference in the frequency of recombination between GLO and HLA was noted, but recom
Publikováno v:
Teratology. 62(6)
Family studies have demonstrated that the autism spectrum disorders (ASDs) have a major genetic etiologic component, but expression and penetrance of the phenotype are variable. Mice with null mutations of Hoxa1 or Hoxb1, two genes critical to hindbr
Autor:
L R, Weitkamp, A J, Moss, R A, Lewis, W J, Hall, J W, MacCluer, P J, Schwartz, E H, Locati, D, Tzivoni, G M, Vincent, J L, Robinson
Publikováno v:
American journal of human genetics. 55(6)
The long-QT (LQT) syndrome is a genetically complex disorder that is characterized by syncope and fatal ventricular arrhythmias. LQT syndrome, as defined by a prolonged electrocardiographic QT interval, has a higher incidence in females than in males
Autor:
L R, Weitkamp, R M, Kenney, E, Bailey, J W, MacCluer, J S, Brown, T L, Blanchard, P L, Sertich, C C, Love, P R, Hunt
Publikováno v:
Journal of reproduction and fertility. Supplement. 44
Histological features of the endometrium, as assessed in biopsy samples, were related to Standardbred mare genotypes for transferrin, esterase (as a control) and equine leucocyte antigens (ELA). Pathological changes were found more frequently in each
Publikováno v:
The Lancet. 351:1554-1555
expected) and T/T homozygotes (18 observed, 29·5 expected). The results were significant both for the 65 spina bifida offspring ( 2=9·66, p=0·0080) and for the 146 unaffected offspring ( 2=9·28, p=0·0097). Taking into account sex, increased hete
Publikováno v:
Neurology. 44:329-329
We report nine additional cases of new-onset multiple sclerosis (MS) among employees of an upstate New York manufacturing plant that uses zinc as a primary metal. These cases, identified during the decade 1980 to 1989, had clinical onset of the disea
Autor:
N.E. Morton, P. Pierce, K. Simola, C.E. Wright, E.J. Yunis, M.E. Chandler, H. Vriesendorp, B.J.B. Keats, C.J. Sherr, K. Bender, R.E. Magenis, H. Oie, B.B. Knowles, J.M. Luciani, M.P. Cowmeadow, I.L. Hansteen, M. Bobrow, G.A. Koch, M. Prensky, P.A. Lalley, N. Shimizu, E.A. Nichols, J. Garver, K. Hirschhorn, A. Brøgger, A.F. Gazdar, S. Hempfling, L.C. Yu, B. Pernis, R. Mausner, S. Leupe-de Smit, R.C.P. Go, A. Westerveld, L. R. Weitkamp, K.E. Toomey, D. Borgaonkar, S. Piomelli, D. Bootsma, T. Campana, E.W. Lovrien, O.J. Miller, H.J. Cooke, F.T. Kao, D.A. Aitken, S. Burgess, L.L. Haley, Y. Boyd, A. Mayerová, T.B. Shows, H.J. Evans, J. Fraisse, K.-H. Grzeschik, V.M. Regina, K.C. Atwood, L.M.M. Wijnen, Liao Law, H.-H. Ropers, M.A. Ferguson-Smith, M.A. Pellegrino, T. Gedde-Dahl, V.A. McKusick, A.C. Leary, J. H. Olving, M.G. Byers, D. Swallow, K.M. Overton, W.F. Witterland, J. Hemmerling, S.J. Funderburk, A. de la Chapelle, N.R. Mendell, U. Francke, Veronica van Heyningen, A.F. Naylor, I.W. Craig, A. Heiberg, R.S. Lemons, J.E. Gray, E. Herbschleb-Voogt, J.J. Yunis, D.B. Amos, C.K. Eun, J.L. Hamerton, L. U. Lamm, N. Oliver, S. Goodnight, F. Pellett, T.M. Dijksman, J.M. Vance, R.E. Eisenman, P. Rubinstein, A. Bratlie, G.A.P. Bruns, V. Kirton, R. Roos, D.L. Slate, M.C. Yoshida, D.L. George, R.C. Schwartz, K.E. Buckton, A.S. Henderson, R. Jonassen, J.A. Robinson, P.L. Pearson, M. Hultén, E. Solomon, A.E. Greene, L.Y. Wang, R. Lange, S. Brown, M.L. Schroeder, P. Karli, A. Krüger, J.M. Robert, B. Lauras, J. Chamberlin, A. Shalev, J. Ott, B.J. Mintz, Elizabeth B. Robson, Per Teisberg, N. Tanigaki, P. M. Conneally, S. Rosenfeld, A.S. Baim, M.L. Rivas, J.A. Brown, R. Johannsmann, N. Suciu-Foca, R. Mierau, T.T. Puck, C.G. Palmer, S.J. Jeremiah, D. Warburton, M. Devictor-Vuillet, J.A. Norton, T. Ho, J.E. Noades, F. Varricchio, E.H.Y. Chu, B. Carritt, R. Schwab, I. Balazs, J. Reiss, C.N. Fear, S. Povey, Erik Thorsby, A. Siverts, D.W. Ball, W. Stanley, L.R. Weitkamp, M.E. Duncan, C. Jones, K. Willecke, S. Philipps, R. Moreland, D.C. Rao, E. Tolley, T. Philip, E. Johnston, M. Monteba-van Heuvel, A.D. Merritt, T.H. Roderick, R.L. Eddy, S. Arias, R.A. Fisher, M.A. Craft, J.H. Edwards, M.C. Sparkes, N.C. Sun, L. Korsnes, D.A. Meyers, M.Y. Tsai, A.W. Johnston, A. Estop, B.M. Turner, K. Berg, S. Guttormsen, W.G. Burgerhout, A.P. Goggin, T. Mohandas, W.K. Stanford, C.W. Bazinet, M. Siniscalco, R.H. Lindenbaum, H.P. Klinger, W.S. Volkers, J. Gavin, K.K. Namboodiri, M.T. Davisson, P.J. McAlpine, W.R.T. Los, M. Meisler, L.J. Donald, F.H. Ruddle, W. Bauch, Timothy A. Donlon, C.R.Y. Sun, R. Bigley, R.S. Sparkes, H. Kaita, P.S. Gerald, E.R. Giblett, I. Berczi, R.C. Elston, S.J. O’Brien, C.T. Falk, L. Scrafford-Wolff, M. Smith, M.K. Fagerhol, J. de Witt, S. Rowe, D. Cox, E.S. Seravalli, T. Borun, M. Lewis, R. Saisson, M.A. Pericak-Vance, R.T. Taggart, R.D.G. McKay, M. Mota, W. R. Mayr, Matthew Parks, F. Freycon, Y. Shimizu, B. Hellkuhl, D.P. Aden, C.A. Slaughter, J.E. Anderson, E. Lovrien, R.M. Denney, N. Lamvik, J. Parekh, B.P. Dorman, A.P.M. Jongsma, M.A. Nijman, C. Verma, J. Wood, M.J. Champion, R. Sanger, A. Bennick, P.L. Yu, A.F. Wilson, W.L. Marsh, L. Pajunen, H. Hameister, B.A. Doppert, J.J. Garver, J.R. Sawyer, P. Meera Khan, P.J.L. Cook, Bjørnar Olaisen, R.C. Karn, J.D. Minna, J.D. Shulkin, B.M. Page, P.M. Sinet, B. Sykes, E.M. Helveston, C.W.H. Partridge, M. Blumenthal, P. Szabo, E.A. Azen
Publikováno v:
Cytogenetic and Genome Research. 22:I-XIV
Autor:
L. R. Weitkamp, R. L. Yagnow, S. A. Guttormsen, Thecla Jorna, C. Flood, Emmanuel Persad, Harvey C. Stancer
Publikováno v:
Genetic Epidemiology. 6:191-194
The Toronto-Rochester Depression study consisted of 116 pedigrees ascertained for multiple cases of major affective disorders. Among the 857 psychiatrically evaluated family members, of whom more than 85% were given a structured interview, 363 had ma
Publikováno v:
Annals of Human Genetics. 41:61-75
SUMMARY An analysis of the linkage relationships of the Hbα, and Hbβ, loci with 34 genetic marker systems is presented. No evidence of linkage of either haemoglobin locus with any of the marker loci was found. The Hbα, locus may be excluded from a