Identification of a mutation in DLX3 associated with tricho-dento-osseous (TDO) syndrome. [electronic resource]
Producer: 19980416Description: 563-9 p. digitalISSN:- 0964-6906
- Abnormalities, Multiple -- genetics
- Amino Acid Sequence
- Animals
- Base Sequence
- Bone and Bones -- abnormalities
- Chromosome Mapping
- Chromosomes, Human, Pair 17
- DNA Mutational Analysis
- Exons
- Genes, Homeobox
- Genetic Markers
- Hair -- abnormalities
- Haplotypes
- Homeodomain Proteins -- chemistry
- Humans
- Mice
- Molecular Sequence Data
- Multigene Family
- Sequence Alignment
- Sequence Homology, Amino Acid
- Syndrome
- Tooth Abnormalities -- genetics
- Transcription Factors -- biosynthesis
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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