Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing. [electronic resource]
Producer: 20120531Description: 599-613 p. digitalISSN:- 1537-6605
- Base Sequence
- Chromosome Breakpoints
- Chromosome Deletion
- Chromosomes, Human, Pair 17 -- genetics
- Comparative Genomic Hybridization -- methods
- DNA Copy Number Variations
- Haplotypes
- Homologous Recombination
- Humans
- Molecular Sequence Data
- Segmental Duplications, Genomic
- Sequence Analysis, DNA -- methods
- Smith-Magenis Syndrome
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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