[Genetic foundation of the beginning of human life]

[Medical applications of genome discovery].

Revista medica de Chile·2002

[History of the scientific work of Eduardo Cruz-Coke Lassabe].

Revista medica de Chile·2001

[UNESCO's bioethical norms to avoid eugenic practices].

Revista medica de Chile·2000

[The history of genetics in Latin American countries during the twentieth century].

Revista medica de Chile·2000

[Hippocratic philosophy].

Revista medica de Chile·1999

[Autonomy accreditation of private Chilean universities (1994-1998)].

Revista medica de Chile·1999

[Recommendation for the recognition, management and follow up of cardiovascular compromise in patients with Pediatric Multisystemic Inflammatory Syndrome associated with COVID-19 (PIMS-CT). Position statement of Chilean Scientific Societies].

Revista chilena de pediatria·2021

[Impact on the quality of life of adolescents with diabetes mellitus type 1].

Revista chilena de pediatria·2021

[The child with persistent stridor].

Revista chilena de pediatria·2021

[Craniosynostosis, a pediatric perspective].

Revista chilena de pediatria·2021

[Brodie's abscess, a pathology difficult to diagnose].

Revista chilena de pediatria·2021

[Influenza A-associated acute necrotizing encephalopathy].

Revista chilena de pediatria·2021

Do not stop at the variant: a reversible cause of small-fiber neuropathy symptoms in an ATTRv carrier.

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology·2026

Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

Genome research·2026

Mutation timing, accumulation, and selection in the male germline shape inheritance risk for developmental disorders.

Cell genomics·2026

Genetics of Educational Attainment and Childhood Problem Behavior: Direct Genetic Effects, Cognitive Pathways, and Sex Differences.

Behavior genetics·2026

Identification of Novel Co-Occurring ZNF711 and SRCAP Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.

The application of clinical genetics·2026

Hox/Meis-dependent gene-regulatory transition underlies cardiopharyngeal neural crest diversification.

The EMBO journal·2026

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[Genetic foundation of the beginning of human life]

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[Medical applications of genome discovery].

[History of the scientific work of Eduardo Cruz-Coke Lassabe].

[UNESCO's bioethical norms to avoid eugenic practices].

[The history of genetics in Latin American countries during the twentieth century].

[Hippocratic philosophy].

[Autonomy accreditation of private Chilean universities (1994-1998)].

[Recommendation for the recognition, management and follow up of cardiovascular compromise in patients with Pediatric Multisystemic Inflammatory Syndrome associated with COVID-19 (PIMS-CT). Position statement of Chilean Scientific Societies].

[Impact on the quality of life of adolescents with diabetes mellitus type 1].

[The child with persistent stridor].

[Craniosynostosis, a pediatric perspective].

[Brodie's abscess, a pathology difficult to diagnose].

[Influenza A-associated acute necrotizing encephalopathy].

Do not stop at the variant: a reversible cause of small-fiber neuropathy symptoms in an ATTRv carrier.

Combined effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system.

Mutation timing, accumulation, and selection in the male germline shape inheritance risk for developmental disorders.

Genetics of Educational Attainment and Childhood Problem Behavior: Direct Genetic Effects, Cognitive Pathways, and Sex Differences.

Identification of Novel Co-Occurring ZNF711 and SRCAP Variants in a Child with Neurodevelopmental Disorders Through Exome Sequencing.

Hox/Meis-dependent gene-regulatory transition underlies cardiopharyngeal neural crest diversification.

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[Genetic foundation of the beginning of human life]

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