Genetics and genomic medicine in Argentina

Evaluating the statistical power of DNA-based identification, exemplified by ‘The missing grandchildren of Argentina’

(2017) Daniel Kling et al.   Forensic Science International-Genetics

Germline hypomorphic CARD11 mutations in severe atopic disease

(2017) Chi A Ma et al.   NATURE GENETICS

Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders

(2017) Dolores González-Morón et al.   PLoS One

Current status of newborn screening worldwide: 2015

(2015) Bradford L. Therrell et al.   SEMINARS IN PERINATOLOGY

Genomic Insights into the Ancestry and Demographic History of South America

(2015) Julian R. Homburger et al.   PLoS Genetics

Whole Genome Sequencing Reveals a De Novo SHANK3 Mutation in Familial Autism Spectrum Disorder

(2015) Sergio I. Nemirovsky et al.   PLoS One

Familias 3 – Extensions and new functionality

(2014) Daniel Kling et al.   Forensic Science International-Genetics

Prevalence and Etiology of Congenital Hypothyroidism Detected through an Argentine Neonatal Screening Program (1997-2010)

(2013) Ana Chiesa et al.   Hormone Research in Paediatrics

Heterogeneity in Genetic Admixture across Different Regions of Argentina

(2012) Sergio Avena et al.   PLoS One