Germline p53 Mutations in a Cohort with Childhood Sarcoma: Sex Differences in Cancer Risk

This publication has 46 references indexed in Scilit:

• Individual-Specific Liability Groups in Genetic Linkage, with Applications to Kindreds with Li-Fraumeni Syndrome
  American Journal of Human Genetics, 2002
• Integrating mutation data and structural analysis of the TP53 tumor-suppressor protein
  Human Mutation, 2002
• Relative frequency and morphology of cancers in carriers of germline TP53 mutations
  Oncogene, 2001
• Detection of 11 germline inactivating TP53 mutations and absence of TP63 and HCHK2 mutations in 17 French families with Li-Fraumeni or Li-Fraumeni-like syndrome
  Journal of Medical Genetics, 2001
• p53 from complexity to simplicity: mutant p53 stabilization, gain‐of‐function, and dominant‐negative effect
  The FASEB Journal, 2000
• p53 compound heterozygosity in a severely affected child with Li-Fraumeni Syndrome
  Oncogene, 1999
• Cancer phenotype correlates with constitutional TP53 genotype in families with the Li–Fraumeni syndrome
  Oncogene, 1998
• Germline p53 mutations are frequently detected in young children with rhabdomyosarcoma.
  Journal of Clinical Investigation, 1995
• Gain of function mutations in p53
  Nature Genetics, 1993
• The Genetic Implications of Long-Term Survival of Childhood Cancer: A Conceptual Framework
  Journal of Pediatric Hematology/Oncology, 1987