Detection of copy number variants in the horse genome and examination of their association with recurrent laryngeal neuropathy-Reference-Cited by-同舟云学术

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Detection of copy number variants in the horse genome and examination of their association with recurrent laryngeal neuropathy

Published:2012-05-14 Issue:2 Volume:44 Page:206-208
ISSN:0268-9146
Container-title:Animal Genetics
language:en
Short-container-title:Anim Genet

Author:

Dupuis M.C.¹²,Zhang Z.¹,Durkin K.¹,Charlier C.¹,Lekeux P.³,Georges M.¹

Affiliation:

1. Unit of Animal Genetics; GIGA-Research; Faculty of Veterinary Medicine; University of Liège; B-4000 Liège Belgium

2. CIRALE (Center of Imaging and Research on Equine Locomotor Affections); National Veterinary School of Alfort; F-14430 Goustranville France

3. Department for Functional Sciences; Faculty of Veterinary Medicine; University of Liège; B-4000 Liège Belgium

Publisher

Wiley

Subject

Genetics,Animal Science and Zoology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2052.2012.02373.x/fullpdf

Reference10 articles.

1. Origins and functional impact of copy number variation in the human genome;Conrad;Nature,2010

2. Results of a haplotype-based GWAS for recurrent laryngeal neuropathy in the horse;Dupuis;Mammalian Genome,2011

3. Serial translocation via circular intermediates underlies color-sidedness in cattle;Durkin;Nature,2012

4. Structural variation in the human genome;Feuk;Nature Reviews Genetics,2006

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