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MeSH Review

Genetics, Population

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Biological context of Genetics, Population


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Gene context of Genetics, Population


Analytical, diagnostic and therapeutic context of Genetics, Population


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  2. Cystic fibrosis mutations and associated haplotypes in Bulgaria - a comparative population genetic study. Angelicheva, D., Calafell, F., Savov, A., Jordanova, A., Kufardjieva, A., Galeva, I., Nedkova, V., Ivanova, T., Yankova, P., Konstantinova, D., Genev, E., Kalaydjieva, L. Hum. Genet. (1997) [Pubmed]
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  4. The evolutionary history of the CCR5-Delta32 HIV-resistance mutation. Galvani, A.P., Novembre, J. Microbes Infect. (2005) [Pubmed]
  5. Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations. Medlej-Hashim, M., Serre, J.L., Corbani, S., Saab, O., Jalkh, N., Delague, V., Chouery, E., Salem, N., Loiselet, J., Lefranc, G., Mégarbané, A. European journal of medical genetics. (2005) [Pubmed]
  6. Functional variants at CYP2A6: new genotyping methods, population genetics, and relevance to studies of tobacco dependence. Zabetian, C.P., Gelernter, J., Cubells, J.F. Am. J. Med. Genet. (2000) [Pubmed]
  7. Microbiology. Bacterial population genetics and disease. Lipsitch, M. Science (2001) [Pubmed]
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  9. Population genetics of CAPN10 and GPR35: implications for the evolution of type 2 diabetes variants. Vander Molen, J., Frisse, L.M., Fullerton, S.M., Qian, Y., Del Bosque-Plata, L., Hudson, R.R., Di Rienzo, A. Am. J. Hum. Genet. (2005) [Pubmed]
  10. Genetic signatures of strong recent positive selection at the lactase gene. Bersaglieri, T., Sabeti, P.C., Patterson, N., Vanderploeg, T., Schaffner, S.F., Drake, J.A., Rhodes, M., Reich, D.E., Hirschhorn, J.N. Am. J. Hum. Genet. (2004) [Pubmed]
  11. Human genetic affinities for Y-chromosome P49a,f/TaqI haplotypes show strong correspondence with linguistics. Poloni, E.S., Semino, O., Passarino, G., Santachiara-Benerecetti, A.S., Dupanloup, I., Langaney, A., Excoffier, L. Am. J. Hum. Genet. (1997) [Pubmed]
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  13. Evolution of a perfect simple sequence repeat locus in the context of its flanking sequence. Blankenship, S.M., May, B., Hedgecock, D. Mol. Biol. Evol. (2002) [Pubmed]
  14. Population genetics of the developmental gene optomotor-blind (omb) in Drosophila polymorpha: evidence for a role in abdominal pigmentation variation. Brisson, J.A., Templeton, A.R., Duncan, I. Genetics (2004) [Pubmed]
  15. Mitochondrial malic enzyme (E.C. in human leukocytes: formal genetics and population genetics. Siebert, G., Ritter, H., Kömpf, J. Hum. Genet. (1979) [Pubmed]
  16. Age and origin of the FCMD 3'-untranslated-region retrotransposal insertion mutation causing Fukuyama-type congenital muscular dystrophy in the Japanese population. Colombo, R., Bignamini, A.A., Carobene, A., Sasaki, J., Tachikawa, M., Kobayashi, K., Toda, T. Hum. Genet. (2000) [Pubmed]
  17. Population genetics of glyoxalase I (E.C. in human erythrocytes. Berg, K., Rodewald, A., Schwarzfischer, F., Wischerath, H. Z. Rechtsmed. (1977) [Pubmed]
  18. Genetic studies of low abundance human plasma proteins. II. Population genetics of coagulation factor XIIIB. Kamboh, M.I., Ferrell, R.E. Am. J. Hum. Genet. (1986) [Pubmed]
  19. Genetic studies of low-abundance human plasma proteins. XIII. Population genetics of C1R complement subcomponent and description of new variants. Kamboh, M.I., Lyons, L.A., Ferrell, R.E. Am. J. Hum. Genet. (1989) [Pubmed]
  20. The confluence of population genetics with molecular pharmacology at the angiotensin II receptor: dawn of a new era or just a new wrinkle? Printz, M.P. Mol. Pharmacol. (2004) [Pubmed]
  21. 17Beta-hydroxysteroid dehydrogenase-3 deficiency: diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations. Boehmer, A.L., Brinkmann, A.O., Sandkuijl, L.A., Halley, D.J., Niermeijer, M.F., Andersson, S., de Jong, F.H., Kayserili, H., de Vroede, M.A., Otten, B.J., Rouwé, C.W., Mendonça, B.B., Rodrigues, C., Bode, H.H., de Ruiter, P.E., Delemarre-van de Waal, H.A., Drop, S.L. J. Clin. Endocrinol. Metab. (1999) [Pubmed]
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  23. A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype. Parasol, N., Reid, M., Rios, M., Castilho, L., Harari, I., Kosower, N.S. Blood (1998) [Pubmed]
  24. Molecular population genetics of ref(2)P, a locus which confers viral resistance in Drosophila. Wayne, M.L., Contamine, D., Kreitman, M. Mol. Biol. Evol. (1996) [Pubmed]
  25. Variant detection at the delta opioid receptor (OPRD1) locus and population genetics of a novel variant affecting protein sequence. Gelernter, J., Kranzler, H.R. Hum. Genet. (2000) [Pubmed]
  26. CTLA-4 and its role in autoimmune thyroid disease. Chistiakov, D.A., Turakulov, R.I. J. Mol. Endocrinol. (2003) [Pubmed]
  27. Molecular analysis of mutations and polymorphisms of the Lewis secretor type alpha(1,2)-fucosyltransferase gene reveals that Taiwan aborigines are of Austronesian derivation. Chang, J.G., Ko, Y.C., Lee, J.C., Chang, S.J., Liu, T.C., Shih, M.C., Peng, C.T. J. Hum. Genet. (2002) [Pubmed]
  28. Evidence for multiple gene loci in the expression of the common generalized epilepsies. Greenberg, D.A., Durner, M., Delgado-Escueta, A.V. Neurology (1992) [Pubmed]
  29. Transferrin (Tf) subtyping on agarose: a new technique for isoelectric focusing. Dykes, D., Polesky, H. Hum. Genet. (1981) [Pubmed]
  30. A molecular analysis of the telomeric end of the major histocompatibility complex. DNA typing of HLA-A3 subtypes and -B7. Dorak, M.T., Wilson, D.W., Galbraith, I., Henderson, N., Burnett, A.K., Worwood, M. Hum. Immunol. (1995) [Pubmed]
  31. Comments on the statistical aspects of the NRC's report on DNA typing. Devlin, B., Risch, N., Roeder, K. J. Forensic Sci. (1994) [Pubmed]
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