Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.
Nolen LD, Amor D, Haywood A, St Heaps L, Willcock C, Mihelec M, Tam P, Billson F, Grigg J, Peters G, Jamieson RV.
Am J Med Genet A. 2006 Aug 15;140(16):1711-8.PMID: 16835935 [PubMed - indexed for MEDLINE]Related articles