Ophthalmic Manifestations of Smith-Magenis Syndrome
- 1 July 1996
- journal article
- review article
- Published by Elsevier in Ophthalmology
- Vol. 103 (7) , 1084-1091
- https://doi.org/10.1016/s0161-6420(96)30563-0
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)American Journal of Medical Genetics, 1996
- Eye abnormalities in the Smith‐Magenis contiguous gene deletion syndromeAmerican Journal of Medical Genetics, 1993
- Smith-Magenis syndrome: a new contiguous gene syndrome. Report of three new cases.Journal of Medical Genetics, 1991
- Clinical and Chromosome Studies of Three Patients with Smith‐Magenis SyndromeDevelopmental Medicine and Child Neurology, 1991
- Contiguous gene syndromes: A component of recognizable syndromesThe Journal of Pediatrics, 1986
- Interstitial deletion of (17)(p11.2p11.2): Report of six additional patients with a new chromosome deletion syndromeAmerican Journal of Medical Genetics, 1986
- Interstitial deletion of (17)(p11.2p11.2) in nine patientsAmerican Journal of Medical Genetics, 1986
- Interstitial deletion of the short arm of chromosome 17Human Genetics, 1984
- The Significance of Spotting of the Iris in MongoloidsArchives of Ophthalmology (1950), 1961
- AGE NORMS OF REFRACTION AND VISIONArchives of Ophthalmology (1950), 1950