Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
1999-6-30
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
1059-7794
pubmed:author
pubmed:issnType
Print
pubmed:volume
Suppl 1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
S62-5
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:9452043-Amino Acid Sequence, pubmed-meshheading:9452043-Amino Acid Substitution, pubmed-meshheading:9452043-Base Sequence, pubmed-meshheading:9452043-Binding Sites, pubmed-meshheading:9452043-DNA, pubmed-meshheading:9452043-DNA Mutational Analysis, pubmed-meshheading:9452043-Family Health, pubmed-meshheading:9452043-Female, pubmed-meshheading:9452043-Humans, pubmed-meshheading:9452043-Male, pubmed-meshheading:9452043-Osteochondrodysplasias, pubmed-meshheading:9452043-Pedigree, pubmed-meshheading:9452043-Point Mutation, pubmed-meshheading:9452043-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:9452043-Protein-Tyrosine Kinases, pubmed-meshheading:9452043-Receptor, Fibroblast Growth Factor, Type 3, pubmed-meshheading:9452043-Receptors, Fibroblast Growth Factor
pubmed:year
1998
pubmed:articleTitle
Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasia.
pubmed:affiliation
MGC Department of Human Genetics and Clinical Genetic Center, Leiden University, The Netherlands.
pubmed:publicationType
Journal Article