Kagami–Ogata syndrome: a clinically recognizable upd(14)pat and related disorder affecting the chromosome 14q32.2 imprinted region

Human chromosome 14q32.2 carries paternally expressed genes including DLK1 and RTL1, and maternally expressed genes including MEG3 and RTL1as, along with the germline-derived DLK1-MEG3 intergenic differentially methylated region (IG-DMR) and the postfertilization-derived MEG3-DMR. Consistent with th...

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Detalles Bibliográficos
Autores principales: Ogata, Tsutomu, Kagami, Masayo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771937/
https://www.ncbi.nlm.nih.gov/pubmed/26377239
http://dx.doi.org/10.1038/jhg.2015.113

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771937/
https://www.ncbi.nlm.nih.gov/pubmed/26377239
http://dx.doi.org/10.1038/jhg.2015.113

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