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Karyotype-phenotype insights from 11q14.1-q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement.
Am J Med Genet A. 2006 Dec 15;140(24):2721-9. doi: 10.1002/ajmg.a.31498.
Am J Med Genet A. 2006.
PMID: 17103440
FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.
Zhang HZ, Li P, Wang D, Huff S, Nimmakayalu M, Qumsiyeh M, Pober BR.
Zhang HZ, et al.
Am J Med Genet A. 2004 Jan 30;124A(3):280-7. doi: 10.1002/ajmg.a.20413.
Am J Med Genet A. 2004.
PMID: 14708101
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