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NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome

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Footnotes

  • This work was supported by the Association Française du Syndrome de Cornélia de Lange (AFSCL). GB was supported by an INSERM fellowship (poste vert); RR by a Sanger Institute Postdoctoral Fellowship; and DS by PHRC grant AOM 02 122.

  • Conflict of interest: none declared.