Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion. [electronic resource]
Producer: 19961213Description: 17-23 p. digitalISSN:- 0888-7543
- Base Sequence
- Chromosome Mapping
- Chromosomes, Human, Pair 7
- Databases, Factual
- Elastin -- genetics
- Female
- Genetic Markers
- Heterozygote
- Humans
- Male
- Molecular Sequence Data
- Polymerase Chain Reaction
- Polymorphism, Genetic
- Repetitive Sequences, Nucleic Acid
- Sequence Deletion
- Sequence Homology, Nucleic Acid
- Williams Syndrome -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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