VIICTR Profiles
ORIT
Pediatrics CRA
Home
About
Overview
Sharing Data
ORCID
Help
History (1)
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions.
See All Pages
Find People
Find Everything
Login
to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
0
)
Return to Top
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions.
RAI1 variations in Smith-Magenis syndrome patients without 17p11.2 deletions. J Med Genet. 2005 Nov; 42(11):820-8.
View in:
PubMed
subject areas
Abnormalities, Multiple
Adolescent
Adult
Animals
Base Sequence
Chromosomes, Human, Pair 17
Craniofacial Abnormalities
Female
Frameshift Mutation
Genetic Variation
Humans
Intellectual Disability
Male
Molecular Sequence Data
Polymorphism, Genetic
Proteins
Self-Injurious Behavior
Syndrome
Trans-Activators
Transcription Factors
authors with profiles
SARAH ELSEA