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- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Congenital Atrichia: A Case Report
- PolyQ length co-evolution in neural proteins
- Hair & Cutaneous Development
- Genome-wide detection of RNA editing events during the hair follicles cycle of Tianzhu white yak
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