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A novel mutation in NIPBL3 in a case of Cornelia de Lange syndrome confirmed with genetic testing following intrauterine fetal death

Research output: Contribution to journalLetterpeer-review

Original languageEnglish
Pages (from-to)283-284
Number of pages2
JournalJournal of Clinical Pathology
Volume67
Issue number3
DOIs
Publication statusPublished - Mar 2014
Externally publishedYes

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