Syndrome de Smith-Magenis
- 1 May 1997
- journal article
- case report
- Published by Elsevier in Archives de Pédiatrie
- Vol. 4 (5) , 438-442
- https://doi.org/10.1016/s0929-693x(97)86671-7
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- Smith-Magenis syndrome deletion: A case with equivocal cytogenetic findings resolved by fluorescence in situ hybridizationAmerican Journal of Medical Genetics, 1995
- Eye abnormalities in the Smith‐Magenis contiguous gene deletion syndromeAmerican Journal of Medical Genetics, 1993
- Confirmation of a particular but nonspecific metacarpophalangeal pattern profile in patients with the Smith‐Magenis syndrome due to interstitial deletion of 17pAmerican Journal of Medical Genetics, 1993
- Physical mapping of microdeletions of the chromosome 17 short arm associated with Smith-Magenis syndromeHuman Genetics, 1993
- Diagnostic hand anomalies in Smith-Magenis syndrome: Four new patients with del (17)(p11.2p11.2)American Journal of Medical Genetics, 1991
- Clinical and Chromosome Studies of Three Patients with Smith‐Magenis SyndromeDevelopmental Medicine and Child Neurology, 1991
- Interstitial deletion of (17)(p11.2p11.2) in nine patientsAmerican Journal of Medical Genetics, 1986