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Authors: Sana Sfar; Abderrazak Abid; Wijden Mahfoudh; Houyem Ouragini; Farah Ouechtati; Sonia Abdelhak; Lotfi Chouchane
Journal: Mol Biol Rep Date: 2008-03-11 Impact factor: 2.316

5. Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

Authors: O Bartsch; W Wuyts; W Van Hul; J T Hecht; P Meinecke; D Hogue; W Werner; B Zabel; G K Hinkel; C M Powell; L G Shaffer; P J Willems
Journal: Am J Hum Genet Date: 1996-04 Impact factor: 11.025

6. The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans.

Authors: G A Clines; J A Ashley; S Shah; M Lovett
Journal: Genome Res Date: 1997-04 Impact factor: 9.043

Bone growth in diaphysial aclasis.

1. HEREDITARY MULTIPLE EXOSTOSIS.

2. Spontaneous resolution of solitary osteochondroma in the young adult.

3. Radiographic findings in hereditary multiple exostoses and a new theory of the pathogenesis of exostoses.

4. Genetic analysis of hereditary multiple exostoses in Tunisian families: a novel frame-shift mutation in the EXT1 gene.

5. Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11.

6. The structure of the human multiple exostoses 2 gene and characterization of homologs in mouse and Caenorhabditis elegans.

7. Spontaneous regression of exostoses: two case reports.

8. Malignant progression in two children with multiple osteochondromas.

9. Multiple osteocartilaginous exostosis. A follow-up study.

10. Correction of knee and ankle valgus in hereditary multiple exostoses using the Ilizarov apparatus.