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    Molin, A., Andrieux, J., Koolen, D. A., Malan, V., Carella, M., Colleaux, L., Cormier-Daire, V., David, A., de Leeuw, N., Delobel, B., Duban-Bedu, B., Fischetto, R., Flinter, F., Kjaergaard, S., Kok, F., Krepischi, A. C., Le Caignec, C., Ogilvie, C. M., Maia, S., Mathieu-Dramard, M., Munnich, A., Palumbo, O., Papadia, F., Pfundt, R., Reardon, W., Receveur, A., Rio, M., Ronsbro Darling, L., Rosenberg, C., Sá, J., Vallee, L., Vincent-Delorme, C., Zelante, L., Bondeson, M., & Annerén, G. (2012). a novel microdeletion syndrome at 3q13.31 characterised by developmental delay, postnatal overgrowth, hypoplastic male genitals, and characteristic facial features. Journal of medical genetics, 49(2), 104–109. http://access.bl.uk/ark:/81055/vdc_100137793231.0x000041
  
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