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APA Citation

    Jacquin, C., Landais, E., Poirsier, C., Afenjar, A., Akhavi, A., Bednarek, N., Bénech, C., Bonnard, A., Bosquet, D., Burglen, L., Callier, P., Chantot‐Bastaraud, S., Coubes, C., Coutton, C., Delobel, B., Descharmes, M., Dupont, J., Gatinois, V., Gruchy, N., Guterman, S., Heddar, A., Herissant, L., Heron, D., Isidor, B., Jaeger, P., Jouret, G., Keren, B., Kuentz, P., Le Caignec, C., Levy, J., Lopez, N., Manssens, Z., Martin‐Coignard, D., Marey, I., Mignot, C., Missirian, C., Pebrel‐Richard, C., Pinson, L., Puechberty, J., Redon, S., Sanlaville, D., Spodenkiewicz, M., Tabet, A., Verloes, A., Vieville, G., Yardin, C., Vialard, F., & Doco‐Fenzy, M. (2023). 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients. American journal of medical genetics, 191(2), 445–458. http://access.bl.uk/ark:/81055/vdc_100173964642.0x000027
  
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