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Trichorhinophalangeal syndrome type III.
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- …
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[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.
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