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A new case of syndromic craniosynostosis with cryptic 19p13.2–p13.13 deletion

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  • How to cite this article: Lysy PA, Ravoet M, Wustefeld S, Bernard P, Nassogne M-C, Wyns E, Sibille C. 2009. A new case of syndromic craniosynostosis with cryptic 19p13.2–p13.13 deletion. Am J Med Genet Part A 149A:2564–2568.

  • Philippe A. Lysy and Marie Ravoet contributed equally to this work.

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