Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. [electronic resource]
Producer: 20130219Description: 2430-8 p. digitalISSN:- 1552-4833
- Adult
- Anterior Eye Segment -- abnormalities
- Cerebellar Diseases -- genetics
- Child, Preschool
- Chromosomes, Human, Pair 6 -- genetics
- Comparative Genomic Hybridization
- Dandy-Walker Syndrome -- genetics
- Eye Abnormalities -- genetics
- Eye Diseases, Hereditary
- Female
- Fetus -- pathology
- Forkhead Transcription Factors -- genetics
- Gene Deletion
- Humans
- In Situ Hybridization, Fluorescence
- Male
- Phenotype
- Pregnancy
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Publication Type: Journal Article
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