Home
About
Overview
Sharing Data
ORCID
Help
History (1)
Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.
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
Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.
Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes. Mol Vis. 2013; 19:759-66.
View in:
PubMed
subject areas
Adolescent
Adult
Aged
Arthritis
Base Sequence
Collagen Type II
Connective Tissue Diseases
DNA Mutational Analysis
DNA, Complementary
Family
Female
Gene Expression Regulation
Hearing Loss, Sensorineural
Humans
Male
Molecular Sequence Data
Mutation
Pedigree
Phenotype
Protein Isoforms
Retinal Degeneration
Retinal Detachment
Versicans
authors with profiles
Tammy L Yanovitch