Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II

Human Genetics

Volumn 114, Issue 5, 2004, Pages 491-498

  Malmgren, Barbro ^a,b   Lindskog, S ^b   Elgadi, A ^a   Norgren, S ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE; GENOMIC DNA; SIGNAL PEPTIDE; VALINE; DSPP PROTEIN, HUMAN; PRIMER DNA; PROTEIN PRECURSOR; SCLEROPROTEIN;

ARTICLE; BLOOD SAMPLING; CASE REPORT; CLINICAL FEATURE; CONTROLLED STUDY; DENTIN; DISEASE SEVERITY; DNA EXTRACTION; DYSPLASIA; FAMILY STUDY; FEMALE; GENETIC ANALYSIS; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MALE; MEDICAL DOCUMENTATION; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE ASSAY; RADIODIAGNOSIS; SCORING SYSTEM; SEQUENCE ANALYSIS; TISSUE SECTION; TOOTH MALFORMATION; CASE CONTROL STUDY; COMPARATIVE STUDY; DNA SEQUENCE; GENETICS; HAPLOTYPE; PATHOLOGY; PEDIGREE; POLYACRYLAMIDE GEL ELECTROPHORESIS; RADIOGRAPHY; SWEDEN; TOOTH;

BASE SEQUENCE; CASE-CONTROL STUDIES; DENTIN; DENTINOGENESIS IMPERFECTA; DNA PRIMERS; ELECTROPHORESIS, POLYACRYLAMIDE GEL; EXTRACELLULAR MATRIX PROTEINS; HAPLOTYPES; HUMANS; MUTATION, MISSENSE; PEDIGREE; PROTEIN PRECURSORS; SEQUENCE ANALYSIS, DNA; SWEDEN; TOOTH;

EID: 2542434141     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-004-1084-z     Document Type: Article

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