Abstract |
The duplication 3q syndrome is characterized by the partial trisomy of a segment of the long arm of chromosome 3. This segment, although variable in size, includes 3q26.3-q27 as the minimal region of overlap. We have previously used patient chromosome breakpoints to select cosmids within this region. In this report, we have used two- and three-color fluorescence in situ hybridization on metaphase and interphase chromosomes to perform high-resolution cytological mapping of the six cosmids identified. The results allowed us to determine the centromere-telomere orientation, the order, and the relative distances of the markers used. Because some of the markers used are part of the consensus chromosome 3 map, our data can be easily integrated with existing mapping information about this chromosome. Our data provide a framework for further physical mapping studies of this region.
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Authors | P Rizzu, A Baldini |
Journal | Genomics
(Genomics)
Vol. 24
Issue 3
Pg. 580-2
(Dec 1994)
ISSN: 0888-7543 [Print] United States |
PMID | 7713511
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
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Topics |
- Abnormalities, Multiple
(genetics)
- Chromosome Aberrations
- Chromosome Banding
- Chromosome Mapping
- Chromosomes, Human, Pair 3
(ultrastructure)
- Cosmids
- DNA
(genetics)
- De Lange Syndrome
(genetics)
- Genetic Markers
- Humans
- In Situ Hybridization, Fluorescence
- Interphase
(genetics)
- Male
- Metaphase
(genetics)
- Syndrome
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