Monnier, C., Dodé, C., Fabre, L., Teixeira, L., Labesse, G., Pin, J., . . . Rondard, P. (2009). PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity. Oxford University Press.

Monnier, Carine, Catherine Dodé, Ludovic Fabre, Luis Teixeira, Gilles Labesse, Jean-Philippe Pin, Jean-Pierre Hardelin, and Philippe Rondard. PROKR2 Missense Mutations Associated With Kallmann Syndrome Impair Receptor Signalling Activity. Oxford University Press, 2009.

Monnier, Carine, et al. PROKR2 Missense Mutations Associated With Kallmann Syndrome Impair Receptor Signalling Activity. Oxford University Press, 2009.