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- Insertional mutation of the hairless locus on mouse Chromosome 14
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Polygenic control of the wavy coat of the NCT mouse: involvement of an intracisternal A particle insertional mutation of the protease, serine 53 (Prss53) gene, and a modifier gene
- Hox demarcates regional regeneration of adult hair follicle stem cells
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Copy number variation regions in Nellore cattle: Evidences of environment adaptation
- A 10 Mb duplication in chromosome band 5q31.3–5q33.1 associated with late-onset lipodystrophy, ichthyosis, epilepsy and glomerulonephritis
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