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1. Generation and comparative analysis of ~3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7qll.23 implicated in Williams syndrome

Author

DeSilva, Udaya, Elnitski, Laura, Idol, Jacquelyn R., Doyle, Johannah L., Gan, Weiniu; ., Green, Eric D., Miller, Webb, Touchman, Jeffrey W., Thomas, Pamela J., Bouffard, Gerard G., Blakesley, Robert W., McDowell, Jennifer C., Beckstrom-Sternberg, Stephen M., Dietriich, Nicole L, Schwartz, Scott;, and Thomas, James W.

Subjects
Developmental disabilities -- Research, Child development deviations -- Research, Human chromosomes -- Research, Williams syndrome -- Research, Genetic research, Health
Abstract

Williams syndrome is a complex developmental disorder that results from the heterozygous deletion of a ~1.6-Mb segment of human chromosome 7qll.23. The results from a study in this context provided an important comparative sequence resource to develop mouse models of the disorder.

Published
2002

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