Comparative genomic hybridization shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations

C. Hernando, A. Plaja, M.A. Rigola, M.M. Perez, T. Vendrell, J. Egozcue, C. Fuster

Research output: Contribution to journalArticleResearch

Original languageEnglish
Pages (from-to)39-41
JournalJ. Med. Genet.
Volume39
Issue number5
Publication statusPublished - 1 Jan 2001

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