A de novo microdeletion in a patient with inner ear abnormalities suggests that the 10q26.13 region contains the responsible gene

Microdeletions in the 10q26.1 region are related to intellectual disability, growth delay, microcephaly, distinctive craniofacial features, cardiac defects, genital abnormalities and inner ear abnormalities. The genes responsible for inner ear abnormalities have been narrowed to fibroblast growth fa...

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Detalles Bibliográficos
Autores principales: Sangu, Noriko, Okamoto, Nobuhiko, Shimojima, Keiko, Ondo, Yumiko, Nishikawa, Masanori, Yamamoto, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Data Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871931/
https://www.ncbi.nlm.nih.gov/pubmed/27274859
http://dx.doi.org/10.1038/hgv.2016.8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4871931/
https://www.ncbi.nlm.nih.gov/pubmed/27274859
http://dx.doi.org/10.1038/hgv.2016.8

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