Comparative Genomic Hybridization of Microdissected Familial Ovarian Carcinoma: Two Deleted Regions on Chromosome 15q Not Previously Identified in Sporadic Ovarian Carcinoma

This publication has 32 references indexed in Scilit:

• Refinement of an ovarian cancer tumour suppressor gene locus on chromosome arm 22q and mutation analysis ofCYP2D6,SREBP2 andNAGA
  International Journal of Cancer, 2000
• Xp22.2-3 Loss of Heterozygosity Is Associated with Germline BRCA1 Mutation in Ovarian Cancer
  Gynecologic Oncology, 2000
• The FEZ1 gene at chromosome 8p22 encodes a leucine-zipper protein, and its expression is altered in multiple human tumors
  Proceedings of the National Academy of Sciences, 1999
• Genetic analysis of 53 lymph node-negative breast carcinomas by CGH and relation to clinical, pathological, morphometric, and DNA cytometric prognostic factors
  The Journal of Pathology, 1998
• A novel candidate tumour suppressor locus at 9q32-33 in bladder cancer: localization of the candidate region within a single 840 kb YAC.
  Human Molecular Genetics, 1997
• Overrepresentation of 3q and 8q material and loss of 18q material are recurrent findings in advanced human ovarian cancer
  Genes, Chromosomes and Cancer, 1996
• Rapid detection of BRCA1 mutations by the protein truncation test
  Nature Genetics, 1995
• Phosphatidylinositol 3‐kinase
  BioEssays, 1994
• Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
  Genes, Chromosomes and Cancer, 1994
• c-myc amplification in ovarian cancer
  Gynecologic Oncology, 1990