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Possible Phenotypic Consequences of Structural Differences in Idic(15) in a Small Cohort of Patients
Among human supernumerary marker chromosomes, the occurrence of isodicentric form of 15 origin is relatively well known due to its high frequency, both in terms of gene content and associated clinical symptoms. The associated epilepsy and autism are typically more severe than in cases with interstit...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801911/ https://www.ncbi.nlm.nih.gov/pubmed/31590400 http://dx.doi.org/10.3390/ijms20194935 |