Works matching DE "MUTATION-selection balance"


Results: 40
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    The Common Ancestor Process Revisited.

    Published in:
    Bulletin of Mathematical Biology, 2013, v. 75, n. 11, p. 2003, doi. 10.1007/s11538-013-9871-0
    By:
    • Kluth, Sandra;
    • Hustedt, Thiemo;
    • Baake, Ellen
    Publication type:
    Article
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    Prenatal genotyping of Gaucher disease in Egypt.

    Published in:
    Egyptian Journal of Medical Human Genetics, 2013, v. 14, n. 4, p. 361, doi. 10.1016/j.ejmhg.2013.06.002
    By:
    • Elgawhary, Somaya;
    • Ghaffar, Hadeer Abdel;
    • Eid, Khaled;
    • Wahab, Magy Abdel;
    • Ragab, Wael Samir;
    • Saleh, Wael Fayek
    Publication type:
    Article
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    Population data for 15 autosomal STR loci from Latvia.

    Published in:
    International Journal of Legal Medicine, 2015, v. 129, n. 4, p. 739, doi. 10.1007/s00414-015-1205-3
    By:
    • Jemeljanova, V.;
    • Gobrusjonoka, O.;
    • Bergere, O.;
    • Latisheva, K.;
    • Axelsson, E.;
    • Pajnič, I.
    Publication type:
    Article
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    Clinical utility gene card for: Cornelia de Lange syndrome.

    Published in:
    European Journal of Human Genetics, 2015, v. 23, n. 10, p. -1, doi. 10.1038/ejhg.2014.270
    By:
    • Ramos, Feliciano J;
    • Puisac, Beatriz;
    • Baquero-Montoya, Carolina;
    • Gil-Rodríguez, Ma Concepción;
    • Bueno, Inés;
    • Deardorff, Matthew A;
    • Hennekam, Raoul C;
    • Kaiser, Frank J;
    • Krantz, Ian D;
    • Musio, Antonio;
    • Selicorni, Angelo;
    • FitzPatrick, David R;
    • Pié, Juan
    Publication type:
    Article
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    Genomic architecture of complex traits in loblolly pine.

    Published in:
    New Phytologist, 2019, v. 221, n. 4, p. 1789, doi. 10.1111/nph.15535
    By:
    • De La Torre, Amanda R.;
    • Puiu, Daniela;
    • Crepeau, Marc W.;
    • Stevens, Kristian;
    • Salzberg, Steven L.;
    • Langley, Charles H.;
    • Neale, David B.
    Publication type:
    Article
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    Letters from Iceland.

    Published in:
    Nature Genetics, 2015, v. 47, n. 5, p. 425, doi. 10.1038/ng.3277
    Publication type:
    Article
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    Exome sequencing identifies recurrent SPOP, FOXA1 and MED12 mutations in prostate cancer.

    Published in:
    Nature Genetics, 2012, v. 44, n. 6, p. 685, doi. 10.1038/ng.2279
    By:
    • Barbieri, Christopher E;
    • Baca, Sylvan C;
    • Lawrence, Michael S;
    • Demichelis, Francesca;
    • Blattner, Mirjam;
    • Theurillat, Jean-Philippe;
    • White, Thomas A;
    • Stojanov, Petar;
    • Van Allen, Eliezer;
    • Stransky, Nicolas;
    • Nickerson, Elizabeth;
    • Chae, Sung-Suk;
    • Boysen, Gunther;
    • Auclair, Daniel;
    • Onofrio, Robert C;
    • Park, Kyung;
    • Kitabayashi, Naoki;
    • MacDonald, Theresa Y;
    • Sheikh, Karen;
    • Vuong, Terry
    Publication type:
    Article
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