P. Faúndez

发表

Myotonic dystrophy in a female with myasthenia gravis.

M. de los Angeles Avaria, K. Kleinsteuber, F. Novoa, 2007, Pediatric neurology.

[Determination of a BRCA1 gene mutation in a family with hereditary breast cancer].

M. Gallardo, P. Faúndez, P. Carvallo, 2004, Revista medica de Chile.

Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype–phenotype correlations

M. King, C. Rousseau, M. Gallardo, 2005, Breast Cancer Research and Treatment.

Promoter hypermethylation of BRCA1 correlates with absence of expression in hereditary breast cancer tumors

L. Solis, A. Corvalán, L. Devoto, 2008, Epigenetics.

Influence of copper-(II) on colloidal carbon-induced Kupffer cell-dependent oxygen uptake in rat liver: relation to hepatotoxicity.

J. Sans, L. Videla, P. Faúndez, 1999, Free radical research.

Genomic rearrangements of the BRCA1 gene in Chilean breast cancer families: an MLPA analysis

P. Faúndez, P. Carvallo, Alejandro Sanchez, 2011, Breast Cancer Research and Treatment.