Associated Papers
A novel TRPS1 mutation in a Chinese patient with trichorhinophalangeal syndrome type I.
Li M et al.
The Journal of Dermatology, 2023
Novel Pathogenetic Variants in PTHLH and TRPS1 Genes Causing Syndromic Brachydactyly.
Elli FM et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research, 2022
34897794 (PubMed )
Supplement: JBMR-37-465-s001.pdf
A novel TRPS1 mutation in a family with tricho-rhino-phalangeal syndrome type 1.
Fujisawa T et al.
The Journal of Dermatology, 2014
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