Fetal growth restriction in a genetic model of sporadic Beckwith–Wiedemann syndrome

Beckwith–Wiedemann syndrome (BWS) is a complex imprinting disorder involving fetal overgrowth and placentomegaly, and is associated with a variety of genetic and epigenetic mutations affecting the expression of imprinted genes on human chromosome 11p15.5. Most BWS cases are linked to loss of methyla...

Descripción completa

Detalles Bibliográficos
Autores principales: Tunster, Simon J., Van de Pette, Mathew, Creeth, Hugo D. J., Lefebvre, Louis, John, Rosalind M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262809/
https://www.ncbi.nlm.nih.gov/pubmed/30158284
http://dx.doi.org/10.1242/dmm.035832

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6262809/
https://www.ncbi.nlm.nih.gov/pubmed/30158284
http://dx.doi.org/10.1242/dmm.035832

Ejemplares similares