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Lidia Marino

Biographic Data

ID8258076
NAMELidia Marino
GIVEN NAMESLidia
FAMILY NAMEMarino
SIGNATUREMARINO L
AFFILIATIONSUniversity of Catania
ORCID0000-0001-6015-3787
VERIFIEDYes
TOTAL WORKS1
TOTAL CITATIONS0
AUTHOR COUNT1
EDITOR COUNT0
FIRST PUBLICATION YEAR2022
LATEST PUBLICATION YEAR2022
H-INDEX0
  • NRXN1 Deletion in Two Twins’ Genotype and Phenotype

    Open Access•Monica Sciacca, Lidia Marino et al.•ARTICLE•Children•2022

    In the literature, deletions in the 2p16.3 region of the neurexin gene (NRXN1) are associated with cognitive impairment, and other neuropsychiatric disorders, such as schizophrenia, autism, and Pitt-Hopkins-like syndrome 2. In this paper, we present twins with deletion 2p16.3 of the NRXN1 gene using a comparative genomic hybridization array. The two children had a dual diagnosis consisting of mild cognitive impairment and neurodevelopmental delay…

No prominent works on this page.

  • NRXN1 Deletion in Two Twins’ Genotype and Phenotype

    Open Access•Monica Sciacca, Lidia Marino et al.•ARTICLE•Children•2022

    In the literature, deletions in the 2p16.3 region of the neurexin gene (NRXN1) are associated with cognitive impairment, and other neuropsychiatric disorders, such as schizophrenia, autism, and Pitt-Hopkins-like syndrome 2. In this paper, we present twins with deletion 2p16.3 of the NRXN1 gene using a comparative genomic hybridization array. The two children had a dual diagnosis consisting of mild cognitive impairment and neurodevelopmental delay…

Assortative mating (1 works) · Autism (1 works) · Bioinformatics (1 works) · Biology (1 works) · Chromosome (1 works) · Cognition (1 works) · Gene (1 works) · Genetic counseling (1 works) · Genetic testing (1 works) · Genetics (1 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae