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Volumn 38, Issue 12, 2001, Pages
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Detection of a large TBX5 deletion in a family with Holt-Oram syndrome.
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Author keywords
[No Author keywords available]
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Indexed keywords
T BOX TRANSCRIPTION FACTOR;
T-BOX TRANSCRIPTION FACTOR 5;
TRANSCRIPTION FACTOR TBX5;
CONGENITAL HEART MALFORMATION;
DOMINANT GENE;
EXON;
FEMALE;
GENE DELETION;
GENETIC SCREENING;
GENETICS;
HUMAN;
LETTER;
LIMB MALFORMATION;
MALE;
NUCLEOTIDE SEQUENCE;
PEDIGREE;
SYNDROME;
DNA MUTATIONAL ANALYSIS;
EXONS;
FEMALE;
GENES, DOMINANT;
GENETIC SCREENING;
HEART DEFECTS, CONGENITAL;
HUMANS;
LIMB DEFORMITIES, CONGENITAL;
MALE;
PEDIGREE;
SEQUENCE DELETION;
SYNDROME;
T-BOX DOMAIN PROTEINS;
MLCS;
MLOWN;
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EID: 0035653535
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.38.12.e44 Document Type: Letter |
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Times cited : (27)
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References (0)
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