| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.3109/07357909409021393 |
| P8608 | Fatcat ID | release_5eglr5b3ibbqpogu6pnzcwyeau |
| P698 | PubMed publication ID | 8281465 |
| P50 | author | Bryan Williams | Q27840138 |
| P2093 | author name string | M J Coppes | |
| P2860 | cites work | Parental imprinting of the mouse H19 gene | Q22122365 |
| Zinc finger point mutations within the WT1 gene in Wilms tumor patients | Q24561664 | ||
| Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development | Q24607161 | ||
| Mutation and cancer: statistical study of retinoblastoma | Q24618185 | ||
| Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus | Q28236741 | ||
| Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping | Q28236877 | ||
| A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease | Q28239519 | ||
| Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor | Q28242483 | ||
| A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma | Q29618817 | ||
| Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells | Q30501796 | ||
| Role for the Wilms tumor gene in genital development? | Q33690707 | ||
| Allele loss on chromosome 16 associated with progression of human hepatocellular carcinoma | Q33772796 | ||
| Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma | Q33853617 | ||
| An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor | Q34189532 | ||
| The candidate Wilms' tumour gene is involved in genitourinary development | Q34189819 | ||
| Structure and expression of the murine retinoblastoma gene and characterization of its encoded protein | Q34299480 | ||
| Regional mapping of the parathyroid hormone gene (PTH) by cytogenetic and molecular studies | Q34530844 | ||
| Uniparental paternal disomy in a genetic cancer-predisposing syndrome | Q34535432 | ||
| A general theory of carcinogenesis | Q34744320 | ||
| Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombination | Q35165770 | ||
| Beckwith-Wiedemann syndrome, tumourigenesis and imprinting | Q35716500 | ||
| Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor | Q36106284 | ||
| Alternative splicing and genomic structure of the Wilms tumor gene WT1 | Q37611742 | ||
| The p53 tumour suppressor gene | Q37751892 | ||
| Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor | Q37874427 | ||
| Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome). | Q37897088 | ||
| Functional inactivation of genes by dominant negative mutations | Q38178605 | ||
| Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence | Q38338176 | ||
| Genomic imprinting and carcinogenesis | Q39466054 | ||
| Experimental reconstruction of mouse eggs and embryos: an analysis of mammalian development | Q39763715 | ||
| Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome | Q40271452 | ||
| Genetics and epidemiology of Wilms' tumor: The French Wilms' tumor study | Q41084456 | ||
| Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor. | Q41174496 | ||
| Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome | Q41660674 | ||
| A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus | Q43430011 | ||
| WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour | Q48206248 | ||
| Human retinoblastoma susceptibility gene: cloning, identification, and sequence | Q48348004 | ||
| Childhood cancer incidence: Geographical and temporal variations | Q48704558 | ||
| Familial predisposition to Wilms tumor does not segregate with the WT1 gene. | Q52049503 | ||
| Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11. | Q52068403 | ||
| Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. | Q52092134 | ||
| Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases. | Q52093151 | ||
| Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development | Q52231802 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus | Q57734356 | ||
| Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare | Q58666719 | ||
| Wilms tumor locus on 11p13 defined by multiple CpG island-associated transcripts | Q58666837 | ||
| Genomic imprinting and embryonal tumours | Q58992891 | ||
| Loss of a Harvey ras allele in sporadic Wilms' tumour | Q59052738 | ||
| Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour | Q59053443 | ||
| Development of homozygosity for chromosome 11p markers in Wilms' tumour | Q59092304 | ||
| Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13 | Q59093972 | ||
| P433 | issue | 1 | |
| P921 | main subject | molecular genetics | Q210506 |
| P304 | page(s) | 57-65 | |
| P577 | publication date | 1994-01-01 | |
| P1433 | published in | Cancer Investigation | Q325953 |
| P1476 | title | The molecular genetics of Wilms tumor | |
| P478 | volume | 12 |
| Q40964154 | Screening for Wilms tumor in high-risk individuals. |
| Q41063796 | The development of the kidney. |
| Q77537840 | Third case of WAGR syndrome with severe obesity and constitutional deletion of chromosome (11)(p12p14) |
| Q33545491 | Wilms' tumor in the adult--report of a case and review of the literature |
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