A non-syndromic intellectual disability associated with a de novo microdeletion at 7q and 18p, microduplication at Xp, and 18q partial trisomy detected using chromosomal microarray analysis approach

BACKGROUND: Chromosome abnormalities that segregate with a disease phenotype can facilitate the identification of disease loci and genes. The relationship between chromosome 18 anomalies with severe intellectual disability has attracted the attention of cytogeneticists worldwide. Duplications of the...

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Detalles Bibliográficos
Autores principales: Pinto, Irene Plaza, Minasi, Lysa Bernardes, da Cruz, Alex Silva, de Melo, Aldaires Vieira, da Cruz e Cunha, Damiana Míriam, Pereira, Rodrigo Roncato, Ribeiro, Cristiano Luiz, da Silva, Claudio Carlos, de Melo e Silva, Daniela, da Cruz, Aparecido Divino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099144/
https://www.ncbi.nlm.nih.gov/pubmed/25028595
http://dx.doi.org/10.1186/1755-8166-7-44

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4099144/
https://www.ncbi.nlm.nih.gov/pubmed/25028595
http://dx.doi.org/10.1186/1755-8166-7-44

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