Fragile X syndrome clinical and associated comorbidities

Clinical and neurophysiological aspects of fragile X syndrome

Fragile X mental retardation 1 gene and metabolic biomarkers in autism and fragile X syndrome

Assessment of antioxidants biomarkers in plasma of Fragile X syndrome patients

Molecular and cytogenetic diagnosis of disorders/differences of sex development: molecular update of genes controlling sexual differentiation

Females with Gonadal Dysgenesis: Cytogenetic and Molecular Analysis

Genetic characterization of a patient with Cornelia de Lange syndrome with a novel missense mutation

Detection of XIST Gene Deletion by Fluorescence in Situ hybridization in Breast Cancer Patients

Study Of The C677T and 1298AC Polymorphic Genotypes Of MTHFR Gene And Phenotype Genotype Correlation In Autism Spectrum Disorder

CYTOGENETIC STUDY OF CHILDREN WITH DEVELOPMENTAL DELAY AND ASSOCIATED ANOMALIES