| scholarly article | Q13442814 |
| P356 | DOI | 10.1111/J.1365-2990.1994.TB00959.X |
| P698 | PubMed publication ID | 8208343 |
| P2093 | author name string | Wiestler OD | |
| Pietsch T | |||
| Giangaspero F | |||
| Kleihues P | |||
| von Deimling A | |||
| Albrecht S | |||
| Brandner S | |||
| P2860 | cites work | Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9 | Q28181962 |
| A dinucleotide repeat polymorphism at the D9S127 locus | Q35060857 | ||
| TP53 tumor suppressor gene: a model for investigating human mutagenesis | Q35323631 | ||
| Dinucleotide repeat polymorphism at the D11S490 locus | Q35896281 | ||
| The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma | Q35993240 | ||
| Cytogenetics and Molecular Genetics of Malignant Gliomas and Medulloblastoma | Q36476788 | ||
| Descriptive epidemiology of primary central nervous system tumours in children: A population-based study | Q36786708 | ||
| Genetic alterations in glioma and medulloblastoma | Q36941609 | ||
| Medulloblastoma: tumor biological and clinical perspectives | Q37386386 | ||
| Chemotherapy for medulloblastoma/primitive neuroectodermal tumors of the posterior fossa | Q37904265 | ||
| Cytogenetics of human brain tumors | Q37934625 | ||
| Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuroma | Q39590706 | ||
| A dinucleotide repeat polymorphism at the D9S109 locus | Q40420451 | ||
| Microsatellite polymorphism at the D9S12 locus | Q40507278 | ||
| Hinfl polymorphism within the 3′ untranslated region of the candidate Wilms tumour gene | Q40532063 | ||
| Location of gene for Gorlin syndrome | Q42452971 | ||
| Construction of a GT polymorphism map of human 9q | Q44680930 | ||
| Deletion mapping of the medulloblastoma locus on chromosome 17p. | Q46677766 | ||
| Chromosome 11p15 deletions in human malignant astrocytomas and primitive neuroectodermal tumors | Q48415494 | ||
| Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction | Q48887616 | ||
| P433 | issue | 1 | |
| P921 | main subject | heterozygosity | Q124059385 |
| P304 | page(s) | 74-81 | |
| P577 | publication date | 1994-02-01 | |
| P1433 | published in | Neuropathology and Applied Neurobiology | Q7002494 |
| P1476 | title | Microsatellite analysis of loss of heterozygosity on chromosomes 9q, 11p and 17p in medulloblastomas | |
| P478 | volume | 20 |
| Q48399835 | AXIN1 mutations but not deletions in cerebellar medulloblastomas |
| Q42815862 | Chromosomal characteristics of childhood brain tumors |
| Q48652929 | Chromosome arm 17p deletion analysis reveals molecular genetic heterogeneity in supratentorial and infratentorial primitive neuroectodermal tumors of the central nervous system |
| Q34783428 | Classifying the medulloblastoma: insights from morphology and molecular genetics |
| Q40376124 | Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma |
| Q34129258 | Comparative genomic hybridization of medulloblastomas and clinical relevance: eleven new cases and a review of the literature |
| Q35796194 | Correlation of loss of heterozygosity at chromosome 9q with histological subtype in medulloblastomas |
| Q24310338 | DMBT1, a new member of the SRCR superfamily, on chromosome 10q25.3-26.1 is deleted in malignant brain tumours |
| Q28277027 | Detection of frameshift mutations of RIZ in gastric cancers with microsatellite instability |
| Q28189231 | Epigenetic silencing of the HIC-1 gene in human medulloblastomas |
| Q41196588 | Genetics of the nevoid basal cell carcinoma syndrome. |
| Q81510539 | Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors |
| Q36645990 | High resolution chromosome 3p, 8p, 9q and 22q allelotyping analysis in the pathogenesis of gallbladder carcinoma |
| Q54751721 | High throughput detection of microsatellite instability by denaturing high-performance liquid chromatography. |
| Q53386081 | Insulin-like growth factor-I receptor - a potential therapeutic target in medulloblastomas. |
| Q70801383 | Isochromosome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system |
| Q35837750 | Medulloblastoma: molecular genetics and animal models |
| Q55476296 | Molecular genetic studies of chromosome 11 and chromosome 22q DNA sequences in pediatric medulloblastomas. |
| Q48465073 | Mutational and expression analysis of the NF1 gene argues against a role as tumor suppressor in sporadic pilocytic astrocytomas |
| Q42436687 | Nevoid basal cell carcinoma syndrome with medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction |
| Q40795419 | Somatic mutations of WNT/wingless signaling pathway components in primitive neuroectodermal tumors |
| Q36422767 | The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma |
| Q36623905 | The molecular pathology of p53 in primitive neuroectodermal tumours of the central nervous system |
| Q41421758 | The nevoid basal cell carcinoma syndrome: genetics and mechanism of carcinogenesis |
| Q41462850 | Towards a unified model of tumor suppression: lessons learned from the human patched gene |
| Q24681580 | Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples |
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