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2006: Nicolas de Roux
GnRH receptor and GPR54 inactivation in isolated gonadotropic deficiency.
Best practice & research. Clinical endocrinology & metabolism 2006;20(4):515-28.
2006: Delphine Zenaty; Patricia Bretones; Cécile Lambe; Isabelle Guemas; Michel David; Juliane Léger; Nicolas de Roux
Paediatric phenotype of Kallmann syndrome due to mutations of fibroblast growth factor receptor 1 (FGFR1).
Molecular and cellular endocrinology 2006;254-255():78-83.
2005: Mireille Castanet; Sylvia Sura-Trueba; Anne Chauty; Aurore Carré; Nicolas de Roux; Simon Heath; Juliane Léger; Stanislas LYONNET; Paul Czernichow; Michel Polak
Linkage and mutational analysis of familial thyroid dysgenesis demonstrate genetic heterogeneity implicating novel genes.
European journal of human genetics : EJHG 2005;13(2):232-9.