Case of 7p22.1 Microduplication Detected by Whole Genome Microarray (REVEAL) in Workup of Child Diagnosed with Autism

Introduction. More than 60 cases of 7p22 duplications and deletions have been reported with over 16 of them occurring without concomitant chromosomal abnormalities. Patient and Methods. We report a 29-month-old male diagnosed with autism. Whole genome chromosome SNP microarray (REVEAL) demonstrated...

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Detalles Bibliográficos
Autores principales: Goitia, Veronica, Oquendo, Marcial, Stratton, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393924/
https://www.ncbi.nlm.nih.gov/pubmed/25893121
http://dx.doi.org/10.1155/2015/212436

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4393924/
https://www.ncbi.nlm.nih.gov/pubmed/25893121
http://dx.doi.org/10.1155/2015/212436

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