Mutation analysis in Indian children with achondroplasia - utility of molecular diagnosis.
Indian J Pediatr
; 2009 Feb; 76(2): 147-9
Article
in En
| IMSEAR
| ID: sea-79213
Full text:
1
Index:
IMSEAR
Main subject:
Achondroplasia
/
Humans
/
DNA Mutational Analysis
/
Child
/
Point Mutation
/
Receptor, Fibroblast Growth Factor, Type 3
/
India
/
Molecular Biology
Country/Region as subject:
Asia
Language:
En
Journal:
Indian J Pediatr
Year:
2009
Type:
Article