Search
forResearch 6
- Current Genetics in Hair Diseases
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Inherited Disorders of the Hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- TONGUE, RED
Learn
— no results
Try a deeper search in learn →Community
— no results
Try a deeper search in community →