| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1050722865 |
| P356 | DOI | 10.1038/SJ.ONC.1201927 |
| P698 | PubMed publication ID | 9690521 |
| P5875 | ResearchGate publication ID | 13593765 |
| P2093 | author name string | Grundy RG | |
| Pritchard J | |||
| Cowell JK | |||
| Scambler P | |||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | heterozygosity | Q124059385 |
| nephroblastoma | Q756289 | ||
| P304 | page(s) | 395-400 | |
| P577 | publication date | 1998-07-01 | |
| P1433 | published in | Oncogene | Q1568657 |
| P1476 | title | Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour. | |
| P478 | volume | 17 |
| Q34841380 | Analysis of wilms tumors using SNP mapping array-based comparative genomic hybridization. |
| Q73758517 | Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18 |
| Q81702106 | Chromosomal alterations in low-grade endometrial stromal sarcoma and undifferentiated endometrial sarcoma as detected by comparative genomic hybridization |
| Q28203320 | Chromosomal organization and localization of the human histone deacetylase 9 gene (HDAC9) |
| Q33875930 | Genetics of Beckwith-Wiedemann syndrome-associated tumors: common genetic pathways |
| Q81510539 | Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors |
| Q55262812 | Germline mutations and somatic inactivation of TRIM28 in Wilms tumour. |
| Q33207533 | Germline mutations of the POU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14. |
| Q36621144 | Loss of heterozygosity at 7p in Wilms' tumour development |
| Q30584951 | Loss of heterozygosity in tumor cells requires re-evaluation: the data are biased by the size-dependent differential sensitivity of allele detection |
| Q74095463 | Low frequency of genetic lesions in Wilms tumors by representational difference analysis |
| Q58493975 | Molecular characterization of a 7p15-21 homozygous deletion in a Wilms tumor |
| Q74189723 | Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia |
| Q35145426 | Presence of vascular anomalies with congenital hemihypertrophy and Wilms tumor: an evidence-based evaluation. |
| Q30464239 | Race disparities in Wilms tumor incidence and biology. |
| Q58813424 | Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours |
| Q34984201 | Renal cancer: cytogenetic and molecular genetic aspects |
| Q44640928 | Subtractive hybridisation screen identifies sexually dimorphic gene expression in the embryonic mouse gonad. |
| Q34181512 | The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour |
| Q84567847 | Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor |
| Q24291145 | VAM-1: a new member of the MAGUK family binds to human Veli-1 through a conserved domain |
| Q34010180 | Wilms tumor genetics: mutations in WT1, WTX, and CTNNB1 account for only about one-third of tumors |
| Q80588993 | Wilms' tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene |
| Q36234726 | Wilms' tumour: connecting tumorigenesis and organ development in the kidney |
Search more.