A 22q11.2 Deletion That Excludes UFD1L and CDC45L in a Patient with Conotruncal and Craniofacial Defects
- 1 August 1999
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 65 (2) , 562-566
- https://doi.org/10.1086/302514
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
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