Are There Low-Penetrance TP53 Alleles? Evidence from Childhood Adrenocortical Tumors
- 1 October 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (4) , 995-1006
- https://doi.org/10.1086/302575
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Cancer phenotype correlates with constitutional TP53 genotype in families with the Li–Fraumeni syndromeOncogene, 1998
- Overview of rb gene mutations in patients with retinoblastomaOphthalmology, 1998
- A novel missense mutation in patients from a retinoblastoma pedigree showing only mild expression of the tumor phenotypeOncogene, 1998
- Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.Journal of Medical Genetics, 1998
- Deletion of RBExons 24 and 25 Causes Low-Penetrance RetinoblastomaAmerican Journal of Human Genetics, 1997
- Rapid Diagnosis of Germline p53 Mutation Using the Enzyme Mismatch Cleavage MethodDiagnostic Molecular Pathology, 1996
- A novel deletion within exon 6 of TP53 in a family with Li-Fraumeni-like syndrome, and LOH in a benign lesion from a mutation carrierCancer Genetics and Cytogenetics, 1996
- An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.Journal of Medical Genetics, 1995
- Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutationsNature Genetics, 1994
- Detection of Novel Germ-line p53 Mutations in Diverse-Cancer-Prone Families Identifiled by Selecting Patients With Childhood Adrencortical CarcinomaJNCI Journal of the National Cancer Institute, 1992