Molecular studies of the circadian control candidate genes in the mouse Smith-Magenis syndrome syntenic region.
The Smith-Magenis syndrome (SMS) is a contiguous gene syndrome which is associated with the deletion in chromosome 17 p11.2. The common clinical features of SMS patients include mental retardation, delayed speech and motor development, behavior problems, sleep disturbance, minor craniofacial abnorma...
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| Format: | Research Report |
| Language: | English |
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2010
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| Online Access: | http://hdl.handle.net/10356/41874 |