Publicaciones en colaboración con investigadores/as de Universidad de Córdoba (5)

2023

  1. Delving into the Genetic Causes of Language Impairment in a Case of Partial Deletion of NRXN1

    Molecular Syndromology, Vol. 13, Núm. 6, pp. 496-510

2022

  1. Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome

    Journal of Speech, Language, and Hearing Research, Vol. 65, Núm. 12, pp. 4724-4740

2021

  1. Language impairment with a microduplication in 1q42.3q43

    Clinical Linguistics and Phonetics, Vol. 35, Núm. 7, pp. 610-635

2020

  1. Language Impairment with a Partial Duplication of DOCK8

    Molecular Syndromology, Vol. 11, Núm. 5-6, pp. 243-263

2018

  1. Narrowing the genetic causes of language dysfunction in the 1q21.1 microduplication syndrome

    Frontiers in Pediatrics, Vol. 6