2014
Recurrent chromosomal aberrations in intravenous leiomyomatosis of the uterus: high-resolution array comparative genomic hybridization study
Buza N, Xu F, Wu W, Carr RJ, Li P, Hui P. Recurrent chromosomal aberrations in intravenous leiomyomatosis of the uterus: high-resolution array comparative genomic hybridization study. Human Pathology 2014, 45: 1885-1892. PMID: 25033729, DOI: 10.1016/j.humpath.2014.05.010.Peer-Reviewed Original ResearchConceptsOligonucleotide array comparative genomic hybridizationArray comparative genomic hybridizationComparative genomic hybridizationGenome-wide investigationGenomic hybridizationChromosome 22qCopy number lossGene mappingChromosomal aberrationsComparative genomic hybridization studySuccinate dehydrogenase subunit BGenetic instabilityRecurrent chromosomal aberrationsRegions of lossSequencing analysisChromosome 12qNumber lossNumber variantsSubunit BChromosomal alterationsHybridization studies
2004
Comparative genomic hybridization study of placental site trophoblastic tumour: a report of four cases
Hui P, Riba A, Pejovic T, Johnson T, Baergen RN, Ward D. Comparative genomic hybridization study of placental site trophoblastic tumour: a report of four cases. Modern Pathology 2004, 17: 248-251. PMID: 14657956, DOI: 10.1038/modpathol.3800025.Peer-Reviewed Original ResearchConceptsPlacental site trophoblastic tumorTrophoblastic tumorChromosomal gainsCases of PSTTComparative genomic hybridizationClinicopathological studyComparative genomic hybridization studyIntermediate trophoblastCase reportNeoplastic proliferationSmall seriesAdditional studiesPathobiological significanceRecurrent chromosomal gainsChromosomal alterationsTumorsChromosomal lossGenomic hybridizationHybridization studiesReport