Incomplete methylation of a germ cell tumor (Seminoma) in a Prader‐Willi male

BACKGROUND: Prader‐Willi syndrome (PWS) is a multisystem genetic disorder characterized by lack of satiety leading to morbid obesity, variable degrees of mental retardation, behavior disorders, short stature, and hypogonadism. The underlying genetic cause for PWS is an imprinting defect resulting fr...

Descripción completa

Detalles Bibliográficos
Autores principales: Eldar‐Geva, Talia, Gross‐Tsur, Varda, Hirsch, Harry J., Altarescu, Gheona, Segal, Reeval, Zeligson, Sharon, Golomb, Eliahu, Epsztejn‐Litman, Silvina, Eiges, Rachel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160713/
https://www.ncbi.nlm.nih.gov/pubmed/30003711
http://dx.doi.org/10.1002/mgg3.448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160713/
https://www.ncbi.nlm.nih.gov/pubmed/30003711
http://dx.doi.org/10.1002/mgg3.448

Ejemplares similares