Genome-Wide Expression Analysis in Fibroblast Cell Lines from Probands with Pallister Killian Syndrome

Pallister Killian syndrome (OMIM: # 601803) is a rare multisystem disorder typically caused by tissue limited mosaic tetrasomy of chromosome 12p (isochromosome 12p). The clinical manifestations of Pallister Killian syndrome are variable with the most common findings including craniofacial dysmorphia...

Descripción completa

Detalles Bibliográficos
Autores principales: Kaur, Maninder, Izumi, Kosuke, Wilkens, Alisha B., Chatfield, Kathryn C., Spinner, Nancy B., Conlin, Laura K., Zhang, Zhe, Krantz, Ian D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199614/
https://www.ncbi.nlm.nih.gov/pubmed/25329894
http://dx.doi.org/10.1371/journal.pone.0108853

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199614/
https://www.ncbi.nlm.nih.gov/pubmed/25329894
http://dx.doi.org/10.1371/journal.pone.0108853

Ejemplares similares