Works matching AU Holl, Heather
Results: 9
Whole genome detection of sequence and structural polymorphism in six diverse horses.
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- PLoS ONE, 2020, v. 15, n. 4, p. 1, doi. 10.1371/journal.pone.0230899
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- Article
A Frameshift Mutation in KIT is Associated with White Spotting in the Arabian Camel.
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- Genes, 2017, v. 8, n. 3, p. 102, doi. 10.3390/genes8030102
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- Article
Generation of a de novo transcriptome from equine lamellar tissue.
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- BMC Genomics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12864-015-1948-8
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- Article
A novel splice mutation within equine KIT and the W15 allele in the homozygous state lead to all white coat color phenotypes.
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- Animal Genetics, 2017, v. 48, n. 4, p. 497, doi. 10.1111/age.12554
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- Article
Novel variants in the KIT and PAX3 genes in horses with white-spotted coat colour phenotypes.
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- Animal Genetics, 2013, v. 44, n. 6, p. 763, doi. 10.1111/age.12057
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- Article
Detection of two equine trisomies using SNP-CGH.
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- Mammalian Genome, 2013, v. 24, n. 5/6, p. 252, doi. 10.1007/s00335-013-9450-6
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- Article
Genome Diversity and the Origin of the Arabian Horse.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66232-1
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- Article
Use of principle component analysis to quantitatively score the equine metabolic syndrome phenotype in an Arabian horse population.
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- PLoS ONE, 2018, v. 13, n. 7, p. 1, doi. 10.1371/journal.pone.0200583
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- Article
Evidence for a Retroviral Insertion in <i>TRPM1</i> as the Cause of Congenital Stationary Night Blindness and Leopard Complex Spotting in the Horse.
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- PLoS ONE, 2013, v. 8, n. 10, p. 1, doi. 10.1371/journal.pone.0078280
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- Article