Interstitial deletion of 6q25.2–q25.3: a novel microdeletion syndrome associated with microcephaly, developmental delay, dysmorphic features and hearing loss
- 26 November 2008
- journal article
- case report
- Published by Springer Science and Business Media LLC in European Journal of Human Genetics
- Vol. 17 (5), 573-581
- https://doi.org/10.1038/ejhg.2008.220
Abstract
No abstract availableThis publication has 31 references indexed in Scilit:
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