Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
Hum Mutat
; 31(10): 1142-54, 2010 Oct.
Article
in En
| MEDLINE
| ID: mdl-20672375
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Abnormalities, Multiple
/
Polydactyly
/
Syndactyly
/
Kruppel-Like Transcription Factors
/
Pallister-Hall Syndrome
/
Mutation
/
Nerve Tissue Proteins
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Hum Mutat
Journal subject:
GENETICA MEDICA
Year:
2010
Type:
Article
Affiliation country:
United States