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Trichorhinophalangeal syndrome type III.
Itin PH, Bohn S, Mathys D, Guggenheim R, Richard G. Itin PH, et al. Dermatology. 1996;193(4):349-52. doi: 10.1159/000246290. Dermatology. 1996. PMID: 8993967 Review.
Trichorhinophalangeal syndrome (TRPS) type III is a newly defined clinical entity. This symptom complex is inherited as an autosomal dominant trait and clinically characterized by growth retardation, craniofacial abnormalities, severe brachydactyly and
Trichorhinophalangeal syndrome (TRPS) type III is a newly defined clinical entity. This symptom complex is inher
The function of TRPS1 in the development and differentiation of bone, kidney, and hair follicles.
Gai Z, Gui T, Muragaki Y. Gai Z, et al. Histol Histopathol. 2011 Jul;26(7):915-21. doi: 10.14670/HH-26.915. Histol Histopathol. 2011. PMID: 21630221 Review.
TRPS1 is a gene involved in Tricho-rhino-phalangeal syndrome (TRPS), an autosomal dominant skeletal disorder. TRPS1 encodes a GATA-type transcription factor that has nine zinc-finger motifs. A variety of mutations in TRPS1 including deletions and insertions, have be …
TRPS1 is a gene involved in Tricho-rhino-phalangeal syndrome (TRPS), an autosomal dominant skeletal disorder. TRPS1 encodes a GATA- …
[Tricho-rhino-phalangeal syndrome, type III].
Makita Y. Makita Y. Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):757-8. Ryoikibetsu Shokogun Shirizu. 2001. PMID: 11529009 Review. Japanese. No abstract available.