4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features
| Autor: | Vande Perre, P., Zazo Seco, C., Patat, O., Bouneau, L., Vigouroux, A., Bourgeois, D., El Hout, S., Chassaing, N., Calvas, P. |
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| Zdroj: | In European Journal of Medical Genetics February 2018 61(2):72-78 |
| Databáze: | ScienceDirect |
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