Incomplete methylation of a germ cell tumor (Seminoma) in a Prader-Willi male

Keyphrases

• Methylation 100%
• Prader-Willi Syndrome 100%
• Germ Cell Tumor 100%
• Seminoma 100%
• Tumor 50%
• Hypogonadism 25%
• Induced Pluripotent Stem Cells (iPSCs) 16%
• Imprinting Center 16%
• Maternal Uniparental Disomy 16%
• Tumor Subtype 8%
• Germ Cells 8%
• Fibroblasts 8%
• Male Patients 8%
• Short Stature 8%
• Haplotype Analysis 8%
• Cell Morphology 8%
• Stem Cell-derived 8%
• Immunostaining 8%
• Genetic Causes 8%
• Specific Events 8%
• Patient Fibroblasts 8%
• Cellular Origin 8%
• Genetic Disease 8%
• Cell Tumor 8%
• Bisulfite 8%
• Locus-specific 8%
• Clinical Expression 8%
• Uniparental Disomy 8%
• Chromosome 15 8%
• Pathological Examination 8%
• Morbid Obesity 8%
• Multisystem 8%
• Behavior Disorders 8%
• Women of Reproductive Age 8%
• DNA Methylation Profiling 8%
• Satiety 8%
• Loss of Methylation 8%
• Germline Specification 8%
• Morphological Type 8%
• Chromosomal Microarray Analysis 8%
• H&E Staining 8%
• Imprinting Defects 8%

Biochemistry, Genetics and Molecular Biology

• Germ Cell 100%
• Methylation 100%
• Prader-Willi Syndrome 100%
• Uniparental Disomy 27%
• Induced Pluripotent Stem Cell 18%
• Fibroblast 18%
• Genetics 9%
• Haplotype 9%
• Wild Type 9%
• DNA Methylation 9%
• Immunostaining 9%
• Genetic Disorder 9%
• Karyotype 9%
• Body Height 9%
• Bisulfite 9%
• Array Comparative Genomic Hybridization 9%
• Chromosome 15 9%
• Satiety 9%
• Cognition 9%
• fertility 9%