- PMID 16528117. "
Trichorhinophalangeal syndrome type ii".
National Organisation for Rare Disorders.
Retrieved July 7, 2021. "
trichorhinophalangeal syndrome type...
-
Trichorhinophalangeal Syndrome Type I (TRPS I) is a rare
genetic disorder characterized by
distinctive craniofacial and
skeletal abnormalities. The name...
-
Trichoodontoonychial dysplasia Trichorhinophalangeal syndrome type I
Trichorhinophalangeal syndrome type II
Trichorhinophalangeal syndrome type III Trichostasis...
- *134450
FACTOR VII REGULATOR; F7R". NCBI/OMIM. "MIM ID #190350
TRICHORHINOPHALANGEAL SYNDROME, TYPE I; TRPS1". NCBI/OMIM. "MIM ID #179613 RECOMBINANT...
-
plasminogen activator TRMT12: tRNA
methyltransferase 12
homolog TRPS1:
trichorhinophalangeal syndrome I TSPYL5 (gene):
encoding protein TSPY like 5 TTI2 encoding...
- on
human chromosome 8q24.1: use in
refining the
location of the
trichorhinophalangeal syndrome and
multiple exostoses genes (TRPS1 and EXT1)". Genomics...
-
Litton JK, Xiao L, et al. (October 2013). "Prognostic
value of the
trichorhinophalangeal syndrome-1 (TRPS-1), a GATA
family transcription factor, in early-stage...
- (ectrodactyly-
ectodermal dysplasia-clefting) syndrome, Neurofibromatosis,
Trichorhinophalangeal syndrome, Trichotillomania, Nail-patella
syndrome and
Woolly hair...
-
voluntary service to the Red Cross.
Sarah Neil. For
services to the
Trichorhinophalangeal Syndrome Support Group.
Michael Kenneth Nicholls. For
services to...
- on
human chromosome 8q24.1: use in
refining the
location of the
trichorhinophalangeal syndrome and
multiple exostoses genes (TRPS1 and EXT1)". Genomics...
