In a shake of a lamb's tail: using genomics to unravel a cause of chondrodysplasia in Texel sheep
Author:
Affiliation:
1. Department of Animal Science and Center for Integrated Animal Genomics; Iowa State University; Ames; IA; 50011; USA
2. Institute of Veterinary, Animal & Biomedical Sciences; Massey University; Palmerston North; 4474; New Zealand
Publisher
Wiley
Subject
Genetics,Animal Science and Zoology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2052.2011.02304.x/fullpdf
Reference33 articles.
1. Microphthalmia in Texel sheep is associated with a missense mutation in the paired-like homeodomain 3 (PITX3) gene;Becker;PLoS One,2010
2. Restriction fragment length polymorphisms in genetic improvement: methodologies, mapping and costs;Beckmann;Theoretical and Applied Genetics,1983
3. A single-base change in the tyrosine kinase II domain of ovine FGFR3 causes hereditary chondrodysplasia in sheep;Beever;Animal Genetics,2006
4. Byrne T.J. 2005 Investigation into the Inheritance and Biochemistry of Chondrodysplasia in Texel Sheep Massey University
5. Inheritance of chondrodysplasia in Texel sheep;Byrne;Proceedings of the New Zealand Society of Animal Production,2008
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