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Works matching AU Pearce, Kerra

Results: 3

1

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

2

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

3

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