Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family. [electronic resource]
Producer: 20041108Description: 1527-33 p. digitalISSN:- 0003-9950
- Adult
- Anterior Chamber -- abnormalities
- Case-Control Studies
- DNA-Binding Proteins -- genetics
- Eye Abnormalities -- genetics
- Family Health
- Female
- Forkhead Transcription Factors
- Genetic Linkage
- Glaucoma -- genetics
- Humans
- Infant
- Male
- Microsatellite Repeats
- Middle Aged
- Mutation, Missense
- Pedigree
- Phenotype
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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