Abnormalities of esophageal transit in patients with sporadic nontoxic goitre

Clonal karyotypic abnormalities of the h

Clonal karyotypic abnormalities of the hereditary multiple exostoses chromosomal loci 8q24.1 (EXT1) and 11p11-12 (EXT2) in patients with sporadic and hereditary osteochondromas

✍ Julia A. Bridge; Mari Nelson; Charlotte Örndal; Paramjit Bhatia; James R. Neff 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 141 KB 👁 3 views

## Background: Osteochondroma most frequently arises sporadically and as a solitary lesion, but also may arise as multiple lesions characterizing the autosomal dominant disorder hereditary multiple exostoses (hme) and the contiguous gene syndromes langer-giedion and defect-11 syndromes. hme is gene