Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Audiology & Neuro-Otology|November 6, 2009
GJB2 and GJB6 genes: molecular study and identification of novel GJB2 mutations in the hearing-impaired Argentinean populationViviana Dalamón, Vanesa Lotersztein, Agustina Béhèran, et al.
Molecular Biology Reports|October 26, 2013
Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate casesViviana Dalamón, M Florencia Wernert, Vanesa Lotersztein, et al.
Molecular Biology Reports|September 13, 2020
Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health systemLucía Daniela Espeche, Andrea Paula Solari, María Ángeles Mori, et al.
Clinical Genetics|August 2, 2024
Identification of copy-number variants in patients with overgrowth disordersAlejandro Parra, Jair Tenorio-Castano, Julián Nevado, et al.
Clinical Epigenetics|April 26, 2026
Investigation of multilocus imprinting disturbance (MLID) in 101 Beckwith-Wiedemann spectrum patientsMario Cazalla, Alejandro Parra, Carlos Rodríguez-Antolín, et al.
NPJ Genomic Medicine|May 22, 2023
Nationwide genetic analysis of more than 600 families with inherited eye diseases in ArgentinaPatricio G Schlottmann, José D Luna, Natalia Labat, et al.
Pageof 2