| P2093 | author name string | Brown KW | |
| | Pires S | |
| | Reynolds PA | |
| | Charles AK | |
| | Malik KT | |
| | Boavida M | |
| | Powlesland RM | |
| P2860 | cites work | Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway | Q24308083 |
| | A genetic model for colorectal tumorigenesis | Q27860582 |
| | A comprehensive genetic map of the human genome based on 5,264 microsatellites | Q27860812 |
| | 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 |
| | Tissue, developmental, and tumor-specific expression of divergent transcripts in Wilms tumor | Q28242483 |
| | Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21 | Q30338283 |
| | Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells | Q30501796 |
| | Wilms' tumour and a de novo (1;7) translocation in a child with bilateral radial aplasia | Q33597093 |
| | Mutation and cancer: a model for Wilms' tumor of the kidney | Q34207334 |
| | Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. | Q35248407 |
| | Microsatellites for linkage analysis of genetic traits | Q35750385 |
| | Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development | Q35753374 |
| | Immunohistochemical detection of p53 in Wilms' tumors correlates with unfavorable outcome. | Q35773597 |
| | Detection of human papillomavirus DNA in biopsies of human oral tissue | Q36029148 |
| | Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors. | Q36435885 |
| | A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps | Q36795131 |
| | Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor | Q37874427 |
| | Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13 | Q40252056 |
| | Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266, and D16S267 loci. | Q40518342 |
| | Constitutional and acquired rearrangements of chromosome 7 in Wilms tumor | Q40541033 |
| | The genetics of Wilms' tumor--a case of disrupted development | Q40614052 |
| | Wilms tumor genes | Q40794258 |
| | Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome | Q41566242 |
| | Renal tumours of childhood | Q43871600 |
| | A YAC contig spanning the dominant retinitis pigmentosa locus (RP9) on chromosome 7p. | Q48071491 |
| | Mutations of the p53 tumor suppressor gene occur infrequently in Wilms' tumor | Q48139314 |
| | Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities. | Q52522804 |
| | Relaxation of imprinted genes in human cancer. | Q52545355 |
| | Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour. | Q55067715 |
| | Characterization of regions of chromosomes 12 and 16 involved in nephroblastoma tumorigenesis | Q57252309 |
| | Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors | Q58813482 |
| | Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11 | Q58813492 |
| | Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour | Q59088779 |
| | Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour | Q59662077 |
| | Involvement of chromosome 7 in Wilms tumor. | Q64930956 |
| | A third Wilms' tumor locus on chromosome 16q | Q67848748 |
| | Chromosome analysis of 31 Wilms' tumors | Q68456578 |
| | Cytogenetic changes in Wilms' tumors | Q69835268 |
| | Constitutional mosaic t(2;7)(q33;p22) and other rearrangements in a girl with Wilms' tumor | Q70091656 |
| | Translocation (7;7)(p13;q21) in a Wilms' tumor | Q70475805 |
| | Isochromosome 7q in adult Wilms' tumor | Q71005959 |
| | Loss of heterozygosity for chromosomes 16q and 1p in Wilms' tumors predicts an adverse outcome | Q72373963 |
| | Simplifying detection of microsatellite length polymorphisms | Q72633431 |
| | Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour | Q72751031 |
| | Germline and somatic abnormalities of chromosome 7 in Wilms' tumor | Q72789607 |
| | Comparative genomic hybridization analysis of Wilms tumors | Q73668835 |
| | Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors | Q74427912 |
| | Novel WT1 mutation, 11p LOH, and t(7;12) (p22;q22) chromosomal translocation identified in a Wilms' tumor case | Q74480214 |
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | heterozygosity | Q124059385 |
| P304 | page(s) | 323-329 | |
| P577 | publication date | 2000-01-01 | |
| P1433 | published in | British Journal of Cancer | Q326309 |
| P1476 | title | Loss of heterozygosity at 7p in Wilms' tumour development | |
| P478 | volume | 82 | |