De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing
Open Access
- 1 May 2014
- journal article
- case report
- Published by Springer Science and Business Media LLC in BMC Medical Genetics
- Vol. 15 (1), 49
- https://doi.org/10.1186/1471-2350-15-49
Abstract
No abstract availableKeywords
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