טוען...
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...
שמור ב:
| הוצא לאור ב: | Mol Genet Genomic Med |
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| Main Authors: | , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2018
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| נושאים: | |
| גישה מקוונת: | 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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