I. Salas

发表

Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome

V. Faundes, M. Field, D. Francis, 2022, American journal of medical genetics. Part A.

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

S. A. Vera, V. Faundes, Alexandra Ure, 2019, Journal of Neurodevelopmental Disorders.

Patients With Fragile X Syndrome Attending a Specialized Centre in Chile: Parent Satisfaction, Costs and Adherence

V. Faundes, P. Morales, S. Aliaga, 2018 .

Clinical, molecular, and pharmacological aspects of FMR1 related disorders.

V. Faundes, S. Aliaga, Á. Pugin, 2017 .

Intellectual functioning and behavioural features associated with mosaicism in fragile X syndrome

S. A. Vera, V. Faundes, Alexandra Ure, 2019, Journal of Neurodevelopmental Disorders.

FMR1 mRNA from full mutation alleles is associated with ABC-CFX scores in males with fragile X syndrome

V. Faundes, Alexandra Ure, M. Field, 2020, Scientific Reports.

Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic features

V. Faundes, K. Cornish, M. Field, 2019, Molecular Autism.

FMR1 gene mutations in patients with fragile X syndrome and obligate carriers: 30 years of experience in Chile.

V. Faundes, P. Morales, S. Aliaga, 2016, Genetics research.

Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt Analysis.

V. Faundes, D. Francis, D. Amor, 2016, Clinical chemistry.