Deletion in 2q35 excluding the IHH gene leads to fetal severe limb anomalies and suggests a disruption of chromatin architecture
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P. Fergelot | P. Pennamen | C. Rooryck | D. Lacombe | Angèle Tingaud-Sequeira | B. Arveiler | J. Bouron | G. André | A. Trimouille | Cécile Boucher