Allelic loss on chromosomes 2q21 and 19p 13.2 in oxyphilic thyroid tumors

Hürthle thyroid tumors are characterized by frequent numerical chromosomal aberrations, including aneuploidy or polyploidy, losses and gains of some chromosomal regions and DNA fragmentation. In recent years, great attention has been paid to the combined analysis of morphologic and genetic features...

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Veröffentlicht in:	International journal of cancer 2004-09, Vol.111 (3), p.463-467
Hauptverfasser:	Stankov, Karmen, Pastore, Alessandro, Toschi, Luca, McKay, James, Lesueur, Fabienne, Kraimps, Jean Louis, Bonneau, Dominique, Gibelin, Hélène, Levillain, Pierre, Volante, Marco, Papotti, Mauro, Romeo, Giovanni
Format:	Artikel
Sprache:	eng
Schlagworte:	19p13.2 2q21 Adenocarcinoma - genetics Chromosome Deletion Chromosome Mapping Chromosomes, Human, Pair 19 - genetics Chromosomes, Human, Pair 2 - genetics Female Genetic Markers Humans Lod Score Loss of Heterozygosity Male microsatellite analysis oxyphilic thyroid tumors Pedigree Thyroid Neoplasms - genetics
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