Variability in clinical phenotype despite common chromosomal deletion in Smith-Magenis syndrome [del(17)(p11.2p11.2)]
- 1 November 2003
- journal article
- research article
- Published by Elsevier BV in Genetics in Medicine
- Vol. 5 (6), 430-434
- https://doi.org/10.1097/01.gim.0000095625.14160.ab
Abstract
No abstract availableKeywords
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