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American Journal of Cardiology, The, ISSN 0002-9149, 2015, Volume 115, Issue 9, pp. 1185 - 1193
Journal Article
Cancer Letters, ISSN 0304-3835, 08/2019, Volume 457, pp. 119 - 128
Wilms tumor is an embryonic renal cancer that typically presents in early childhood and accounts for 7% of all paediatric cancers. Different genetic... 
Epigenetic mutations | Nephroblastoma | Genomic imprinting | IMPRINTING CENTER | SUPPRESSOR GENE | PROMOTER METHYLATION | GROWTH-FACTOR-II | FREQUENT EVENT | CHROMOSOME ARM 16Q | WT1 GENE | BECKWITH-WIEDEMANN-SYNDROME | ONCOLOGY | INSULATOR PROTEIN CTCF | EXPRESSION | Epigenetic inheritance | Research institutes | Methylation | DNA | Cancer
Journal Article
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 06/2015, Volume 60, Issue 6, pp. 287 - 293
Silver-Russell syndrome (SRS) is a heterogeneous disorder characterized by intrauterine and post-natal growth retardation, dysmorphic facial features and body... 
RETARDATION | GROWTH | GENETICS & HEREDITY | 12Q14 MICRODELETION SYNDROME | COMMON | SHORT STATURE | HEIGHT | OSTEOPOIKILOSIS | Sequence Deletion | RNA Splice Sites | Genetic Association Studies | Humans | Child, Preschool | Case-Control Studies | Silver-Russell Syndrome - genetics | Phenotype | DNA Mutational Analysis | Pedigree | Base Sequence | HMGA2 Protein - genetics | Female | Mutation
Journal Article
European journal of human genetics, ISSN 1018-4813, 2009, Volume 17, Issue 5, pp. 611 - 619
Journal Article
Journal Article