Group: CGREL - with tag 1-geneticdiversity1999 [13 articles] Export

Recent papers posted by members of the CGREL group with tag 1-geneticdiversity1999

	combined use of biallelic and microsatellite y-chormosome polymorphisms to infer affinities among african populations [My Copy] by Scozzari, Cruciani, Santolamazza, et al. Malaspina, Torroni, Sellitto, Arredi, Destro-Bisol, De Stefano, Rickards, Martinez-Labarga, Modiano, Biondi, Moral, Olckers, Wallace, Novelletto posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 18:00:08 as
	peopling of sahul: mtdna variation in aboriginal austrailian and papua new guinean populations [My Copy] by A. Redd, M. Stoneking posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:57:10 as
	prevalence and phenotype consequence of fraxa and fraxe alleles in a large, ethically diverse special education-needs population [My Copy] by Crawford, Meadows, Newman, et al. Taft, Pettay, Gold, Hershey, Hinkle, Stanfield, Holmgreen, Yeargin-Allsopp, Boyle, Sherman posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:55:41 as
	The prevelance of common BRCA1 and BRCA 2 Mutations among ashkenazi jews [My Copy] by Hatge, Struewing, Wacholder, Brody, Tucker posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:52:56 as
	Ancestral asian sources of new world y-chromosome founder haplotypes [My Copy] by Tm Karafet, Zegura, Posukh, et al.L. Osipova, B. Long, L. Goldman, Kiltz, De Knijff, Harihara, Wiebe, Griffiths, Templeton, Hammer posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:51:20 as
	The origins of Hypertrophic Cardiomyopathy-causing mutations in two south african subpopulations: a unique profile of both independent and founder events [My Copy] by Moolman-Smook, de Lange, Bruwer, Brink, Corfield posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:48:32 as
	Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population. [My Copy] Am J Hum Genet, Vol. 64, No. 4. (April 1999), pp. 949-962. by I. Aksentijevich, Y. Torosyan, J. Samuels, et al.M. Centola, E. Pras, J. J. Chae, C. Oddoux, G. Wood, M. P. Azzaro, G. Palumbo, R. Giustolisi, M. Pras, H. Ostrer, D. L. Kastner posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:46:17 as
	The central siberian origin for native american y chromosomes [My Copy] by Santos, Pandya, Tyler-Smith, et al. Pena, Schanfield, Leonard, Osipova, Crawford, Mitchell posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:44:50 as
	linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in mexican americans [My Copy] by Duggirala, Blangero, L. Almasy, et al. Dyer, Williams, R. Leach, P. O'Connell, Stern posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:43:15 as
	Structure of the gene congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations [My Copy] by Lenkkeri, Mannikko, Mccready, et al. Lamerdin, Gribouval, Niaudet, Antignac, Kashtan, Homberg, Olsen, Kestila, Tyggvason posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:38:22 as
	iemann-pick c1 disease: the I1061T Substitution is a frequent mutant allele in patients of western european descent and correlates with a classic juvenile phenotype [My Copy] by Millat, Marcais, Rafi, et al. Yamamoto, Morris, Pentchev, Ohno, Wenger, Vanier posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:36:26 as
	A genomewide screen for schizophrenia genes in an isloated finnish subpopulation, suggesting multiple susceptibility loci [My Copy] by Hovatta, Varilo, Suvisaari, et al. Terwilliger, Ollikainen, Arajarvi, Juvonen, Ml Kokko-Sahin, Vaisanen, Mannila, Lonnqvist, Peltonen posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:32:09 as
	A genomewide Analysis provides evidence for novel linkages in inflammatory bowel disease in large european cohort [My Copy] by Hampe, Schreiber, Shaw, et al. Lau, Bridger, Macpherson, Cardon, Sadul, Harris, Buckler, Hall, Stokkers, Jh van Deventer, Nurnberg, Mirza, Lee, Lennard-Jones, Mathew, Curran posted to 1-geneticdiversity1999 by cgreal to the group CGREL on 2007-05-03 17:28:54 as

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Group: CGREL - with tag 1-geneticdiversity1999 [13 articles] Export

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