Expression of SIX3, ZFP161 and ALK Genes in the Brain and Kidneys of3H1 Br Mutant Mice
A newly identified mouse mutation, called Br, displays heritable phenotypic features of frontonasal dysplasia (FND) and multic0ystic renal hypodysplasia (MRHD). The Br mutation is mapped to distal murine chromosome 17, but the causative gene remains unknown. The objective of this project was to anal...
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University of Hawaii at Manoa
2009
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| Online Access: | http://hdl.handle.net/10125/6950 |