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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Mol Genet Genomic Med
Egile Nagusiak: Eldar‐Geva, Talia, Gross‐Tsur, Varda, Hirsch, Harry J., Altarescu, Gheona, Segal, Reeval, Zeligson, Sharon, Golomb, Eliahu, Epsztejn‐Litman, Silvina, Eiges, Rachel
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: John Wiley and Sons Inc. 2018
Gaiak:
Original Articles
Sarrera elektronikoa: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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