Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements. [electronic resource]
Producer: 20040412Description: 198-206 p. digitalISSN:- 0340-6717
- Chromosome Aberrations
- Chromosome Banding
- Chromosome Disorders
- Chromosome Mapping
- Chromosomes, Human, Pair 1 -- genetics
- Cytogenetic Analysis -- methods
- DNA -- genetics
- DNA Probes
- DNA Replication -- genetics
- Gene Deletion
- Gene Rearrangement
- Humans
- In Situ Hybridization, Fluorescence
- Monosomy -- genetics
- Repetitive Sequences, Nucleic Acid -- genetics
- Telomere -- genetics
- Translocation, Genetic
No physical items for this record
Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.