Cargando…
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...
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: | |
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 |
Ejemplares similares
-
A 15q14 microdeletion involving MEIS2 identified in a patient with autism spectrum disorder
por: Shimojima, Keiko, et al.
Publicado: (2017) -
A 7q31.33q32.1 microdeletion including LRRC4 and GRM8 is associated with severe intellectual disability and characteristics of autism
por: Sangu, Noriko, et al.
Publicado: (2017) -
Infantile spasms related to a 5q31.2-q31.3 microdeletion including PURA
por: Shimojima, Keiko, et al.
Publicado: (2018) -
Myopia in Chinese families shows linkage to 10q26.13
por: Musolf, Anthony M., et al.
Publicado: (2018) -
A de novo microdeletion involving PAFAH1B (LIS1) related to lissencephaly phenotype
por: Shimojima, Keiko, et al.
Publicado: (2015)