Comparison of benign and malignant follicular thyroid tumours by comparative genomic hybridization

This publication has 20 references indexed in Scilit:

• Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides.
  1997
• Frequent Loss of Heterozygosity on Chromosomes 3p and 17p without VHL or p53 Mutations Suggests Involvement of Unidentified Tumor Suppressor Genes in Follicular Thyroid Carcinoma1
  Journal of Clinical Endocrinology & Metabolism, 1997
• Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesothelioma
  British Journal of Cancer, 1997
• Loss of heterozygosity at chromosome regions 22q11–12 and 11p15.5 in renal rhabdoid tumors
  Genes, Chromosomes and Cancer, 1996
• Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas
  Nature Genetics, 1994
• Abnormalities of chromosome 22 in meningiomas and confirmation of the origin of a dicentric 22 by in situ hybridization
  Cancer Genetics and Cytogenetics, 1992
• Cytogenetic and molecular genetic studies of follicular and papillary thyroid cancers.
  Journal of Clinical Investigation, 1991
• Cytogenetics of thyroid follicular adenomas
  Cancer Genetics and Cytogenetics, 1990
• The WHO histological classification of thyroid tumors: A commentary on the second edition
  Cancer, 1989
• Classification and prognosis of thyroid carcinoma: A study of 885 cases observed in a thirty year period
  The American Journal of Surgery, 1961