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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Mol Genet Genomic Med
Hlavní autoři: Eldar‐Geva, Talia, Gross‐Tsur, Varda, Hirsch, Harry J., Altarescu, Gheona, Segal, Reeval, Zeligson, Sharon, Golomb, Eliahu, Epsztejn‐Litman, Silvina, Eiges, Rachel
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2018
Témata:
Original Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6160713/
https://ncbi.nlm.nih.gov/pubmed/30003711
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.448
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky