An Interstitial Deletion at 10q26.2q26.3

We present a case of an interstitial subtelomeric 10q26 deletion in a male child with moderate developmental delay and minor dysmorphic features. Using array comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH), we have detected an interstitial deletion at 10q26.2q26...

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Detalles Bibliográficos
Autores principales: Iourov, Ivan Y., Vorsanova, Svetlana G., Kurinnaia, Oxana S., Yurov, Yuri B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932651/
https://www.ncbi.nlm.nih.gov/pubmed/24649379
http://dx.doi.org/10.1155/2014/505832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932651/
https://www.ncbi.nlm.nih.gov/pubmed/24649379
http://dx.doi.org/10.1155/2014/505832

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