| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF01194272 |
| P698 | PubMed publication ID | 7798299 |
| P50 | author | Chiara Menin | Q56849203 |
| P2093 | author name string | E D'Andrea | |
| L Chieco-Bianchi | |||
| M Montagna | |||
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Constitutional relaxation of insulin-like growth factor II gene imprinting associated with Wilms' tumour and gigantism | Q24337027 | ||
| The product of the H19 gene may function as an RNA | Q24599284 | ||
| Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11 | Q28267975 | ||
| A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting | Q30450833 | ||
| Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma | Q33853617 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Imprinting of human H19: allele-specific CpG methylation, loss of the active allele in Wilms tumor, and potential for somatic allele switching | Q35194604 | ||
| Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. | Q35248366 | ||
| Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome. A new case and review of the literature | Q36731805 | ||
| Report of the committee on the genetic constitution of chromosome 11. | Q37782382 | ||
| Genomic imprinting and carcinogenesis | Q39466054 | ||
| Dinucleotide repeat polymorphism at the IGF2R locus | Q40420425 | ||
| Loss of alleles on the short arm of chromosome 11 in a hepatoblastoma from a child with Beckwith-Wiedemann syndrome. | Q41335659 | ||
| Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome | Q41523994 | ||
| Preferential loss of maternal alleles in sporadic Wilms' tumour. | Q45004084 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Embryological and molecular investigations of parental imprinting on mouse chromosome 7. | Q55052972 | ||
| The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans | Q58061470 | ||
| Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism | Q59053447 | ||
| Loss of genes on the short arm of chromosome 11 in bladder cancer | Q59066203 | ||
| Tumour-suppressor activity of H19 RNA | Q59071440 | ||
| Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 | ||
| Three non-overlapping regions of chromosome arm 11p allele loss identified in infantile tumors of adrenal and liver | Q60212965 | ||
| Generation of homozygosity at the c-Ha-ras-1 locus on chromosome 11p in an adrenal adenoma from an adult with Wiedemann—Beckwith syndrome | Q60212968 | ||
| Molecular differential pathology of rhabdomyosarcoma | Q69149585 | ||
| Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours | Q69844381 | ||
| A routine method for the establishment of permanent growing lymphoblastoid cell lines | Q70146139 | ||
| Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma | Q70147637 | ||
| P433 | issue | 12 | |
| P921 | main subject | heterozygosity | Q124059385 |
| P304 | page(s) | 732-736 | |
| P577 | publication date | 1994-01-01 | |
| P1433 | published in | Journal of Cancer Research and Clinical Oncology | Q2081599 |
| P1476 | title | Occasional loss of constitutive heterozygosity at 11p15.5 and imprinting relaxation of the IGFII maternal allele in hepatoblastoma | |
| P478 | volume | 120 |
| Q30865178 | Altered expression of members of the IGF-axis in hepatoblastomas |
| Q64245279 | CircHMGCS1 Promotes Hepatoblastoma Cell Proliferation by Regulating the IGF Signaling Pathway and Glutaminolysis |
| Q36622040 | Comparative genomic hybridization reveals population-based genetic alterations in hepatoblastomas |
| Q28268815 | Expression profiling and differential screening between hepatoblastomas and the corresponding normal livers: identification of high expression of the PLK1 oncogene as a poor-prognostic indicator of hepatoblastomas |
| Q28140252 | Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma |
| Q33875930 | Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways |
| Q33721384 | Genomic imprinting and chromatin insulation in Beckwith-Wiedemann syndrome |
| Q42056824 | Loss of heterozygosity on chromosome 11p15 during histological progression in microdissected ductal carcinoma of the breast |
| Q37010551 | Loss of imprinting of IGF2 correlates with hypermethylation of the H19 differentially methylated region in hepatoblastoma |
| Q35212566 | The Wnt signaling pathway in solid childhood tumors |
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