Mutations in the fibroblast growth factor receptor 3 (FGFR3) cause achondroplasia, hypochondroplasia, and thanatophoric dysplasia: Taiwanese data [1]

American Journal of Medical Genetics

Volumn 86, Issue 3, 1999, Pages 300-301

  Tsai, F J ^a   Tsai, C H ^a   Chang, J G ^a   Wu, J Y ^a  

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

FIBROBLAST GROWTH FACTOR RECEPTOR;

ACHONDROPLASIA; BONE DYSPLASIA; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HYPOCHONDROPLASIA; LETTER; PRIORITY JOURNAL; TAIWAN; THANATOPHORIC DWARFISM;

ACHONDROPLASIA; BASE SEQUENCE; DNA PRIMERS; HUMANS; POINT MUTATION; PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3; RECEPTORS, FIBROBLAST GROWTH FACTOR; TAIWAN; THANATOPHORIC DYSPLASIA;

EID: 0032829239     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990917)86:3<300::AID-AJMG21>3.0.CO;2-H     Document Type: Letter

References (5)