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Genes, Chromosomes & Cancer|March 1, 1994
Numerical chromosomal aberrations in thyroid tumors detected by double fluorescence in situ hybridizationD Taruscio, M L Carcangiu, T Ried, et al.Proceedings of the National Academy of Sciences of the United States of America|February 15, 1992
Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopyT Ried, A Baldini, T C Rand, et al.Cell Death and Differentiation|February 24, 2007
Haploinsufficiency of Parp1 accelerates Brca1-associated centrosome amplification, telomere shortening, genetic instability, apoptosis, and embryonic lethalityX Wang, L Liu, C Montagna, et al.Human Molecular Genetics|August 1, 1992
Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cellsT Ried, G Landes, W Dackowski, et al.Prenatal Diagnosis|June 9, 1999
Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotypingY Ning, C H Laundon, E Schröck, et al.Journal of Molecular Endocrinology|June 1, 1994
Localization of the human FSH receptor to chromosome 2 p21 using a genomic probe comprising exon 10J Gromoll, T Ried, H Holtgreve-Grez, et al.Genes, Chromosomes & Cancer|June 24, 1999
Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlationT Ried, K Heselmeyer-Haddad, H Blegen, et al.Nature Genetics|April 1, 1997
Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotypingT Veldman, C Vignon, E Schröck, et al.Genomics|August 1, 1992
Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomesP Lichter, P Bray, T Ried, et al.Oral Oncology|September 21, 2001
Abnormal DNA content predicts the occurrence of carcinomas in non-dysplastic oral white patchesJ Sudbø, T Ried, M Bryne, et al.Pageof 13