Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response

BACKGROUND: Despite the extensive use of chromosomal microarray technologies in patients with neurodevelopmental disorders has permitted the identification of an increasing number of causative submicroscopic rearrangements throughout the genome, constitutional duplications involving chromosome 1q22...

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Detalles Bibliográficos
Autores principales: Fichera, Marco, Barone, Rita, Grillo, Lucia, De Grandi, Mariaclara, Fiore, Valerio, Morana, Ignazio, Maniscalchi, Tiziana, Vinci, Mirella, Amata, Silvestra, Spalletta, Angela, Sorge, Giovanni, Signorelli, Salvatore Santo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276019/
https://www.ncbi.nlm.nih.gov/pubmed/25540671
http://dx.doi.org/10.1186/s13039-014-0090-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4276019/
https://www.ncbi.nlm.nih.gov/pubmed/25540671
http://dx.doi.org/10.1186/s13039-014-0090-7

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