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    Xu, C., Cassatella, D., van der Sloot, A., Quinton, R., Hauschild, M., De Geyter, C., Flück, C., Feller, K., Bartholdi, D., Nemeth, A., Halperin, I., Pekic Djurdjevic, S., Maeder, P., Papadakis, G., Dwyer, A., Marino, L., Favre, L., Pignatelli, D., Niederländer, N., Acierno, J., & Pitteloud, N. (2018). evaluating CHARGE syndrome in congenital hypogonadotropic hypogonadism patients harboring CHD7 variants. Genetics in medicine, 20, 872–881. http://access.bl.uk/ark:/81055/vdc_100086850527.0x0000c3
  
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