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

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Footnotes

  • Contributors All authors included on this article fulfil the criteria of authorship. All have been involved in the clinical care of the family and in the revision of this article. Dr Robertson has taken overall responsibility for the content.

  • Competing interests None.

  • Patient consent Obtained.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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    BMJ Publishing Group Ltd and Association of Clinical Pathologists