Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases. [electronic resource]
Producer: 20000614Description: 432-9 p. digitalISSN:- 0340-6717
- Amino Acid Sequence
- Animals
- Blepharophimosis -- genetics
- Blepharoptosis -- genetics
- Charcot-Marie-Tooth Disease -- genetics
- Chick Embryo
- Chromosome Mapping
- Chromosomes, Human, Pair 3
- Eye Abnormalities -- genetics
- Genetic Testing
- High Mobility Group Proteins -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Mice
- Mobius Syndrome -- genetics
- Molecular Sequence Data
- Mutation
- SOXB2 Transcription Factors
- Sequence Homology, Amino Acid
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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