Identification of a common N540K mutation in 8/18 Taiwanese hypochondroplasia patients: Further evidence for genetic heterogeneity [2]

Clinical Genetics

Volumn 55, Issue 4, 1999, Pages 279-280

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

^a CHINA MEDICAL UNIVERSITY HOSPITAL   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; HUMAN CELL; HYPOCHONDROPLASIA; LETTER; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

BASE SEQUENCE; DNA PRIMERS; GENETIC HETEROGENEITY; HUMANS; MUTATION; OSTEOCHONDRODYSPLASIAS; POLYMERASE CHAIN REACTION; PROTEIN-TYROSINE KINASES; RECEPTOR, FIBROBLAST GROWTH FACTOR, TYPE 3; RECEPTORS, FIBROBLAST GROWTH FACTOR; TAIWAN;

EID: 0032966496     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.1999.550412.x     Document Type: Letter

References (45)