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...

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Bibliografske podrobnosti
izdano v:Mol Genet Genomic Med
Main Authors: Eldar‐Geva, Talia, Gross‐Tsur, Varda, Hirsch, Harry J., Altarescu, Gheona, Segal, Reeval, Zeligson, Sharon, Golomb, Eliahu, Epsztejn‐Litman, Silvina, Eiges, Rachel
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2018
Teme:
Original Articles
Online dostop: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
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