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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Dades bibliogràfiques
Publicat a:Mol Genet Genomic Med
Autors principals: Eldar‐Geva, Talia, Gross‐Tsur, Varda, Hirsch, Harry J., Altarescu, Gheona, Segal, Reeval, Zeligson, Sharon, Golomb, Eliahu, Epsztejn‐Litman, Silvina, Eiges, Rachel
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Original Articles
Accés en línia: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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