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...

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Detalles Bibliográficos
Autores principales: Czakó, Márta, Till, Ágnes, Szabó, András, Ripszám, Réka, Melegh, Béla, Hadzsiev, Kinga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801911/
https://www.ncbi.nlm.nih.gov/pubmed/31590400
http://dx.doi.org/10.3390/ijms20194935

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