FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference47 articles.
1. Developmental abnormalities associated with long arm deletion of chromosome No. 6
2. Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome
3. Integration of the Cytogenetic, Genetic, and Physical Maps of the Human Genome by FISH Mapping of CEPH YAC Clones
4. A Novel Locus for Autosomal Dominant Nonsyndromic Hearing Loss, DFNA13, Maps to Chromosome 6p
5. Ring chromosome 6 in a child with minimal abnormalities
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