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- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- The accelerated aging skin in rhino‐like SHJH<sup><i>hr</i></sup> mice
- Meibomian gland changes in the rhino (hrrhhrrh) mouse.
- The abnormal, mis-localizated HR bmh protein associates with members of the protein processing machinery in the cytoplasm
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
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