Novel TBX5 mutations and molecular mechanism for Holt-Oram syndrome.

Journal of medical genetics

Volumn 40, Issue 3, 2003, Pages

  Fan, C ^a   Duhagon, M A ^a   Oberti, C ^a   Chen, S ^a   Hiroi, Y ^a   Komuro, I ^a   Duhagon, P I ^a   Canessa, R ^a   Wang, Q ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ATRIAL NATRIURETIC FACTOR; DNA; HYBRID PROTEIN; LUCIFERASE; T BOX TRANSCRIPTION FACTOR; T-BOX TRANSCRIPTION FACTOR 5; TRANSCRIPTION FACTOR TBX5;

ACTIVE TRANSPORT; ANIMAL; ARTICLE; CELL LINE; CELL NUCLEUS; CELL STRAIN 3T3; CHEMISTRY; CONGENITAL HEART MALFORMATION; FAMILY HEALTH; FEMALE; GENE DELETION; GENETICS; HUMAN; LIMB MALFORMATION; MALE; METABOLISM; MOLECULAR GENETICS; MOUSE; MULTIPLE MALFORMATION SYNDROME; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PEDIGREE; PROMOTER REGION; PROTEIN BINDING; STOP CODON; SYNDROME;

3T3 CELLS; ABNORMALITIES, MULTIPLE; ACTIVE TRANSPORT, CELL NUCLEUS; ANIMALS; ATRIAL NATRIURETIC FACTOR; BASE SEQUENCE; CELL LINE; CELL NUCLEUS; CODON, NONSENSE; DNA; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; LIMB DEFORMITIES, CONGENITAL; LUCIFERASES; MALE; MICE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PROMOTER REGIONS (GENETICS); PROTEIN BINDING; RECOMBINANT FUSION PROTEINS; SEQUENCE DELETION; SYNDROME; T-BOX DOMAIN PROTEINS;

EID: 0037362522     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.3.e29     Document Type: Article

References (0)