Clinical and molecular characterization of a patient with an interstitial deletion of chromosome 12q15-q23 and peripheral corneal abnormalities. [electronic resource]
Producer: 20060327Description: 566-567 p. digitalISSN:- 0002-9394
- Adult
- Calcineurin -- genetics
- Carrier Proteins -- genetics
- Child, Preschool
- Chromosome Deletion
- Chromosomes, Human, Pair 12 -- genetics
- Cornea -- abnormalities
- Corneal Dystrophies, Hereditary -- genetics
- Female
- Genetic Linkage
- Humans
- Male
- Membrane Proteins -- genetics
- Microsatellite Repeats
- Myopia -- genetics
- Proteoglycans -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural
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