Angelman Syndrome due to familial translocation: unexpected additional results characterized by Microarray-based Comparative Genomic Hybridization

BACKGROUND: The 15q11q13 region is subject to imprinting and is involved in various structural rearrangements. Less than 1% of Angelman Syndrome patients are due to translocations involving 15q11q13. These translocations can arise de novo or result from the segregation of chromosomes involved in a f...

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Detalles Bibliográficos
Autores principales: Yokoyama-Rebollar, Emiy, Ruiz-Herrera, Adriana, Lieberman-Hernández, Esther, Del Castillo-Ruiz, Victoria, Sánchez-Sandoval, Silvia, Ávila-Flores, Silvia M, Castrillo, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404657/
https://www.ncbi.nlm.nih.gov/pubmed/25901183
http://dx.doi.org/10.1186/s13039-015-0127-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404657/
https://www.ncbi.nlm.nih.gov/pubmed/25901183
http://dx.doi.org/10.1186/s13039-015-0127-6

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