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Revista Medica De Chile|April 29, 2011
[Molecular and genetic studies for hereditary colon cancer in two patients and their families]Teresa Aravena, Cristóbal Passalacqua, Silvia Castillo Taucher
American Journal of Medical Genetics. Part A|September 13, 2011
Two sisters resembling Gorlin-Chaudhry-Moss syndromeTeresa Aravena, Cristóbal Passalacqua, Oscar Pizarro, et al.
Pediatric Neurology|February 26, 2005
Williams syndrome: pediatric, neurologic, and cognitive developmentXimena Carrasco, Silvia Castillo, Teresa Aravena, et al.
Consciousness and Cognition|February 2, 2010
ADHD children outperform normal children in an artificial grammar Implicit learning task: ERP and RT evidenceRicardo Rosas, Francisco Ceric, Marcela Tenorio, et al.
Revista Medica De Chile|August 27, 2002
[Williams syndrome: clinical, cytogenetical, neurophysiological and neuroanatomic study]Teresa Aravena, Silvia Castillo, Ximena Carrasco, et al.
Revista Medica De Chile|September 24, 2004
[Mutational analysis of the muscle segment homeobox gene 1 (MSX1) in Chilean patients with cleft lip/palate]Alexandre R Vieira, Silvia Castillo Taucher, Teresa Aravena, et al.
Biological Research|February 9, 2010
VEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based studyJuan Francisco Calderón, Alonso R Puga, M Luisa Guzmán, et al.
Revista Chilena De Pediatria|May 29, 2016
[Congenital anomalies of poor prognosis. Genetics Consensus Committee]Rosa A Pardo Vargas, Mariana Aracena, Teresa Aravena, et al.
American Journal of Medical Genetics. Part A|October 15, 2013
Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrumCristina Gervasini, Silvia Russo, Anna Cereda, et al.
Hormone Research in Paediatrics|September 5, 2015
A Deletion of More than 800 kb Is the Most Recurrent Mutation in Chilean Patients with SHOX Gene DefectsHelena Poggi, Alejandra Vera, Carolina Avalos, et al.
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