Found: 3

Select item for more details and to access through your institution.

  • Novel mutations in LHX3 are associated with hypopituitarism and sensorineural hearing loss.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 14, p. 2150, doi. 10.1093/hmg/ddn114
    By:
    • Rajab, Anna;
    • Kelberman, Daniel;
    • de Castro, Sandra C.P.;
    • Biebermann, Heike;
    • Shaikh, Hala;
    • Pearce, Kerra;
    • Hall, Catherine M.;
    • Shaikh, Guftar;
    • Gerrelli, Dianne;
    • Grueters, Annette;
    • Krude, Heiko;
    • Dattani, Mehul T.
    Publication type:
    Article

  • Identification of mutations in CUL7 in 3-M syndrome.

    Published in:
    Nature Genetics, 2005, v. 37, n. 10, p. 1119, doi. 10.1038/ng1628
    By:
    • Huber, Céline;
    • Dias-Santagata, Dora;
    • Glaser, Anna;
    • O'Sullivan, James;
    • Brauner, Raja;
    • Wu, Kenneth;
    • Xinsong Xu;
    • Pearce, Kerra;
    • Rong Wang;
    • Uzielli, Maria Luisa Giovannucci;
    • Dagoneau, Nathalie;
    • Chemaitilly, Wassim;
    • Superti-Furga, Andrea;
    • Dos Santos, Heloisa;
    • Mégarbané, André;
    • Morin, Gilles;
    • Gillessen-Kaesbach, Gabriele;
    • Hennekam, Raoul;
    • van der Burgt, Ineke;
    • Black, Graeme C. M.
    Publication type:
    Article

  • Genomic Risk Profiling of Ischemic Stroke: Results of an International Genome-Wide Association Meta-Analysis.

    Published in:
    PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0023161
    By:
    • Meschia, James F.;
    • Singleton, Andrew;
    • Nalls, Michael A.;
    • Rich, Stephen S.;
    • Sharma, Pankaj;
    • Ferrucci, Luigi;
    • Matarin, Mar;
    • Hernandez, Dena G.;
    • Pearce, Kerra;
    • Brott, Thomas G.;
    • Brown Jr., Robert D.;
    • Hardy, John;
    • Worrall, Bradford B.
    Publication type:
    Article