| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1014288260 |
| P356 | DOI | 10.1023/A:1006387518100 |
| P698 | PubMed publication ID | 10619495 |
| P2093 | author name string | G Vassal | |
| A Lellouch-Tubiana | |||
| C Besnard-Guerin | |||
| S Lescop | |||
| P2860 | cites work | Microsatellite analysis of childhood brain tumors | Q71574842 |
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| Replication errors in hematological neoplasias: genomic instability in progression of disease is different among different types of leukemia | Q77557571 | ||
| Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis | Q22122362 | ||
| Microsatellite instability in cancer of the proximal colon | Q29620692 | ||
| Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma | Q30502386 | ||
| Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32. | Q34490781 | ||
| Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. | Q35248366 | ||
| Genetic linkage of Beckwith-Wiedemann syndrome to 11p15. | Q35248407 | ||
| Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer | Q35477427 | ||
| Microsatellite instability and mutation of DNA mismatch repair genes in gliomas. | Q35753493 | ||
| Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas | Q35796194 | ||
| Instability of microsatellites in human gliomas. | Q40607686 | ||
| Molecular analysis of childhood primitive neuroectodermal tumors defines markers associated with poor outcome | Q40851117 | ||
| A high resolution CEPH crossover mapping panel and integrated map of chromosome 11. | Q40925596 | ||
| The genomic organization and expression of the WT1 gene | Q41120172 | ||
| Paediatric brain tumours | Q41352944 | ||
| Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas | Q41489842 | ||
| Sporadic medulloblastomas contain PTCH mutations. | Q42434884 | ||
| Medulloblastomas of the desmoplastic variant carry mutations of the human homologue of Drosophila patched. | Q42439709 | ||
| Mutations in the human homologue of the Drosophila segment polarity gene patched (PTCH) in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system. | Q42440473 | ||
| Clues to the pathogenesis of familial colorectal cancer | Q42622043 | ||
| Loss of heterozygosity on 6q, 16q, and 17p in human central nervous system primitive neuroectodermal tumors | Q43742822 | ||
| Deletion within the D17S34 locus in a primitive neuroectodermal tumor | Q46230242 | ||
| Reduction to homozygosity and gene amplification in central nervous system primitive neuroectodermal tumors of childhood | Q46491507 | ||
| Structural chromosomal abnormalities in human medulloblastoma | Q48125276 | ||
| Chromosome abnormalities in pediatric brain tumors | Q48135652 | ||
| Instability of short tandem repeats (microsatellites) in human cancers. | Q48181678 | ||
| Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors | Q48415494 | ||
| Molecular analysis of a partial deletion of 22q in a central nervous system rhabdoid tumor | Q48440019 | ||
| Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors. | Q48468591 | ||
| High-resolution deletion mapping of chromosome arm 17p in childhood primitive neuroectodermal tumors reveals a common chromosomal disruption within the Smith-Magenis region, an unstable region in chromosome band 17p11.2. | Q48822376 | ||
| Loss of genetic information in central nervous system tumors common to children and young adults | Q48946826 | ||
| Microsatellite instability analysis of primary human brain tumors. | Q49013311 | ||
| Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours. | Q52092134 | ||
| Analysis of microsatellite repeats in pediatric brain tumors. | Q53461067 | ||
| Microsatellite instability and mutated type II transforming growth factor-beta receptor gene in gliomas. | Q55478796 | ||
| Loss of heterozygosity at locus F13B on chromosome 1q in human medulloblastoma. | Q55479413 | ||
| Frequent loss of heterozygosity on chromosome 9, and low incidence of mutations of cyclin-dependent kinase inhibitors p15 (MTS2) and p16 (MTS1) genes in gliomas | Q55480556 | ||
| Loss of heterozygosity at 11p15 in malignant glioma. | Q55480780 | ||
| Infrequent p53 gene mutations in medulloblastomas. | Q55483960 | ||
| Clonal genomic alterations in glioma malignancy stages. | Q55486049 | ||
| Reduction to homozygosity of genes on chromosome 11 in human breast neoplasia | Q57287881 | ||
| Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour | Q59053443 | ||
| Chromosomal localization of the human rhabdomyosarcoma locus by mitotic recombination mapping | Q59093916 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 119-127 | |
| P577 | publication date | 1999-09-01 | |
| P1433 | published in | Journal of Neuro-Oncology | Q15752119 |
| P1476 | title | Molecular genetic studies of chromosome 11 and chromosome 22q DNA sequences in pediatric medulloblastomas. | |
| P478 | volume | 44 |
| Q55474087 | Aberrant promoter methylation of previously unidentified target genes is a common abnormality in medulloblastomas--implications for tumor biology and potential clinical utility. |
| Q40376124 | Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma |
| Q48185234 | Genome wide copy number abnormalities in pediatric medulloblastomas as assessed by array comparative genome hybridization |
| Q33864635 | Identification and characterization of KCASH2 and KCASH3, 2 novel Cullin3 adaptors suppressing histone deacetylase and Hedgehog activity in medulloblastoma. |
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