1. Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases. Issue 9 (September 1996) Authors: Pivnick, E K; Velagaleti, G V; Wilroy, R S; Smith, M E; Rose, S R; Tipton, R E; Tharapel, A T Journal: Journal of medical genetics Issue: Volume 33:Issue 9(1996) Page Start: 772 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗