By Robert S. Krauss (Eds.)
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Extra resources for Mouse Models of Developmental Genetic Disease
Mol. Teratol. 79, 187–210. Haycraft, C. , et al. (2005). Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet. 1, e53. , et al. (1995). Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice. Nat. Genet. 11, 60–63. Hol, F. , et al. (1995). A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome. J. Med. Genet. 32, 52–56.
Et al. (1995). Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice. Nat. Genet. 11, 60–63. Hol, F. , et al. (1995). A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome. J. Med. Genet. 32, 52–56. Hol, F. , et al. (1996). PAX genes and human neural tube defects: An amino acid substitution in PAX1 in a patient with spina bifida. J. Med. Genet. 33, 655–660. Hoth, C. , et al. (1993). Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I).
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Mouse Models of Developmental Genetic Disease by Robert S. Krauss (Eds.)