MeSH Review:
Musculoskeletal Abnormalities
- Familial hypertryptophanemia in two siblings. Martin, J.R., Mellor, C.S., Fraser, F.C. Clin. Genet. (1995)
- Enteropathic arthropathies. Björkengren, A.G., Resnick, D., Sartoris, D.J. Radiol. Clin. North Am. (1987)
- Wrinkly skin syndrome: phenotype and additional manifestations. Casamassima, A.C., Wesson, S.K., Conlon, C.J., Weiss, F.H. Am. J. Med. Genet. (1987)
- Kabuki syndrome is not caused by a microdeletion in the DiGeorge/velocardiofacial chromosomal region within 22q 11.2. Li, M., Zackai, E.H., Niikawa, N., Kaplan, P., Driscoll, D.A. Am. J. Med. Genet. (1996)
- Prevalence of mitral-valve prolapse in the Stickler syndrome. Liberfarb, R.M., Goldblatt, A. Am. J. Med. Genet. (1986)
- Unilateral athelia with a subcutaneous dermoid cyst. Hosokawa, K., Hata, Y., Yano, K., Susuki, T., Kikui, T., Tahara, S. Plast. Reconstr. Surg. (1987)
- Musculoskeletal abnormalities in velocardiofacial syndrome. Pollard, M.E., Cushing, M.V., Ogden, J.A. Journal of pediatric orthopedics. (1999)
- A study of a family with inherited disease of cardiac and skeletal muscle. Part I. Clinical, electrocardiographic, echocardiographic, haemodynamic, electrophysiological and electron microscopic studies. Przybojewski, J.Z., Hoffman, H., de Graaf, A.S., van der Walt, J.J., Tiedt, F.A., O'Kennedy, A., Torrington, M., Lochner, A., Hewlett, R. S. Afr. Med. J. (1981)