EGAGenomicsCancer Genomicshttps://ega-archive.org/studies/EGAS00001002171EGAEGA study EGAS00001002171Pre-clinical evolution of haematological malignancies_WGSSomatic genetic basis of Wilms’ tumourDetection of cancer cell transcriptomesSingle cell atlas of neuroblastoma and the human fetal adrenal glandSingle cell study of infant leukemiasCongenital mesoblastic nephroma and infantile fibrosarcomaPhylogenetic development of childhood tumoursEGArestrictedCXXC9, DNA (cytosine-5)-methyltransferase 1, DNMT1, study, ADCADN, UNQ203/PRO229, CT-2, HSN1E, DNMT1_HUMAN, Genomes, cell process disease, tumor disease, DNA (cytosine-5-)-methyltransferase 1, neoplasia, Neoplasms, neoplasm (disease), DNMT, neoplastic disease, tumour, MCMT, Tumor, disease of cellular proliferation, CXXC-type zinc finger protein 9, tumours, API6, MALIGNANT AND UNSPECIFIED (INCL CYSTS AND POLYPS), Aim, AIM, neoplastic growth, DNA methyltransferase HsaI, NEOPL., rare (European definition), tumor, other neoplasm, CXXC finger protein 9, neoplasm, CLEC2C, NEOPLASMS BENIGN, Neoplastic Growth, Neoplasia, m.HsaI, DNA MTase HsaI, Tumorsstudy, Neuroblastoma (Schwannian Stroma-Poor), neuroblastoma, Neuroblastomas, Orphaned Child, Neuroblastoma, Orphaned, Central neuroblastoma, familial, Children, neuroblastoma (morphologic abnormality), Sympathicoblastoma, genetic, [M]Neuroblastoma NOS (morphologic abnormality), Orphan, Orphans, Orphaned Children, (Neuroblastoma NOS) or (sympathicoblastoma), [M]Neuroblastoma NOS, neuroblastoma NOS (morphologic abnormality)., NOS, inherited genetic, NB, NB - Neuroblastoma, other neoplasm, constitutitional genetic, hereditaryfalseOrphan Tumour Study familial neuroblastomaThe aim of this study is to study the genomes of ultra rare childhood tumours2022-07-05 14:41:51EGAS000010021719606EGAD00001007853EGAD00001008345EGAD00001006423EGAD00001003884EGAD00001005770EGAD00001009005EGAD00001004774EGAC00001000000EGAC00001000205