subject area of
- A FISH study of chromosome fusion in the ICF syndrome: involvement of paracentric heterochromatin but not of the centromeres themselves. Journal Articles
- A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization Journal Articles
- Amplified sequences from chromosome 15, including centromeres, nucleolar organizer regions, and centromeric heterochromatin, in homogeneously staining regions in the human melanoma cell line MeWo Journal Articles
- Chromosome 17 centromere (CEP17) duplication as a predictor of anthracycline response: evidence from the NCIC Clinical Trials Group (NCIC CTG) MA.5 Trial Journal Articles
- Control of Centromere Localization of the MEI-S332 Cohesion Protection Protein Journal Articles
- Detection of novel centromeric polymorphisms associated with alpha satellite DNA from human chromosome 11 Journal Articles
- Detection of restriction fragment length polymorphisms at the centromeres of human chromosomes by using chromosome-specific alpha satellite DNA probes: implications for development of centromere-based genetic linkage maps. Journal Articles
- Gene for von Recklinghausen Neurofibromatosis Is in the Pericentromeric Region of Chromosome 17 Journal Articles
- Genome sequence of the Brown Norway rat yields insights into mammalian evolution Journal Articles
- Identification of a megaplasmid centromere reveals genetic structural diversity within the repABC family of basic replicons Journal Articles
- Mutations in the Drosophila Condensin Subunit dCAP-G Journal Articles
- Nonrandom localization of recombination events in human alpha satellite repeat unit variants: implications for higher-order structural characteristics within centromeric heterochromatin. Journal Articles
- Organization and genomic distribution of ?82H? alpha satellite DNA Journal Articles
- Rearrangements of chromosomal regions containing ribosomal RNA genes and centromeric heterochromatin in the human melanoma cell line MeWo Journal Articles
- Separation anxiety at the centromere Journal Articles
- Unusual dicentric chromosome 22 associated with a 22q13 deletion Journal Articles