-
1
-
-
84856541750
-
Heritability of recurrent laryngeal neuropathy
-
(Ed. by C. Tessier & V. Gerber), Berne, Switzerland
-
Barakzai S., (2009) Heritability of recurrent laryngeal neuropathy. In: Fourth World Equine Airways Symposium (Ed. by, C. Tessier, &, V. Gerber,), pp. 40-2. Berne, Switzerland, www.ivis.org.
-
(2009)
Fourth World Equine Airways Symposium
, pp. 40-42
-
-
Barakzai, S.1
-
2
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
Conrad D.F., Pinto D., Redon R., et al,. (2010) Origins and functional impact of copy number variation in the human genome. Nature 464, 704-12.
-
(2010)
Nature
, vol.464
, pp. 704-712
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
-
3
-
-
80054761711
-
Results of a haplotype-based GWAS for recurrent laryngeal neuropathy in the horse
-
Dupuis M.C., Zhang Z., Druet T., et al,. (2011) Results of a haplotype-based GWAS for recurrent laryngeal neuropathy in the horse. Mammalian Genome 22, 613-20.
-
(2011)
Mammalian Genome
, vol.22
, pp. 613-620
-
-
Dupuis, M.C.1
Zhang, Z.2
Druet, T.3
-
4
-
-
84863043816
-
Serial translocation via circular intermediates underlies color-sidedness in cattle
-
Durkin K., Coppieters W., Drögemüller C., et al,. (2012) Serial translocation via circular intermediates underlies color-sidedness in cattle. Nature 482, 81-4.
-
(2012)
Nature
, vol.482
, pp. 81-84
-
-
Durkin, K.1
Coppieters, W.2
Drögemüller, C.3
-
5
-
-
31144469134
-
Structural variation in the human genome
-
DOI 10.1038/nrg1767, PII NRG1767
-
Feuk L., Carson A.R., &, Scherer S.W., (2006) Structural variation in the human genome. Nature Reviews Genetics 7, 85-97. (Pubitemid 43128895)
-
(2006)
Nature Reviews Genetics
, vol.7
, Issue.2
, pp. 85-97
-
-
Feuk, L.1
Carson, A.R.2
Scherer, S.W.3
-
6
-
-
24044448222
-
Estimation of heritability of laryngeal Hemiplegia in the Thoroughbred horse by gibbs sampling
-
DOI 10.1294/jes.14.81
-
Ibi T., Miyake T., Hobo S., et al,. (2003) Estimation of heritability of laryngeal hemiplegia in the Thoroughbred horse by Gibbs sampling. Journal of Equine Science 14, 81-6. (Pubitemid 41215298)
-
(2003)
Journal of Equine Science
, vol.14
, Issue.3
, pp. 81-86
-
-
Ibi, T.1
Miyake, T.2
Hobo, S.3
Oki, H.4
Ishida, N.5
Sasaki, Y.6
-
7
-
-
33846703963
-
Genetic basis of respiratory disorders
-
(Ed. by P. Lekeux) International Veterinary Information Service, Ithaca, NY
-
Marti E., &, Ohnesorge B., (2002) Genetic basis of respiratory disorders. In: Equine Respiratory Diseases (Ed. by, P. Lekeux,) International Veterinary Information Service, Ithaca, NY, www.ivis.org.
-
(2002)
Equine Respiratory Diseases
-
-
Marti, E.1
Ohnesorge, B.2
-
8
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon R., Ishikawa S., Fitch K.R., et al,. (2006) Global variation in copy number in the human genome. Nature 444, 444-54. (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
9
-
-
10344256146
-
Consensus statements on equine recurrent laryngeal neuropathy: Conclusions of the Havemeyer Workshop
-
Robinson N.E., (2004) Consensus statements on equine recurrent laryngeal neuropathy: conclusions of the Havemeyer Workshop. Equine Veterinary Education 16, 333-6.
-
(2004)
Equine Veterinary Education
, vol.16
, pp. 333-336
-
-
Robinson, N.E.1
-
10
-
-
35948984173
-
PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data
-
DOI 10.1101/gr.6861907
-
Wang K., Li M., Hadley D., Liu R., et al,. (2007) penncnv: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. Genome Research 17, 1665-74. (Pubitemid 350074862)
-
(2007)
Genome Research
, vol.17
, Issue.11
, pp. 1665-1674
-
-
Wang, K.1
Li, M.2
Hadley, D.3
Liu, R.4
Glessner, J.5
Grant, S.F.A.6
Hakonarson, H.7
Bucan, M.8
|