Author:
Selzer Rebecca R.,Richmond Todd A.,Pofahl Nathan J.,Green Roland D.,Eis Peggy S.,Nair Prakash,Brothman Arthur R.,Stallings Raymond L.
Reference40 articles.
1. The breakpoint region of the most common isochromosome, i(17q), in human neoplasia is characterized by a complex genomic architecture with large, palindromic, low-copy repeats;Barbouti;Am J Hum Genet,2004
2. Comparative genomic hybridization using oligonucleotide microarrays and total genomic DNA;Barrett;Proc Natl Acad Sci USA,2004
3. Coordinate deletion of chromosome 3p and 11q in neuroblastoma detected by comparative genomic hybridization;Breen;Cancer Genet Cytogenet,2000
4. High-resolution global profiling of genomic alterations with long oligonucleotide microarray;Brennan;Cancer Res,2004
5. Chromosome 1p allelic loss in neuroblastoma: prognosis, genomic imprinting and 1;17 translocations;Caron;Prog Clin Biol Res,1994
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