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Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Dodé C, Levilliers J, Dupont JM, De Paepe A, Le Dû N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pêcheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP. Dodé C, et al. Among authors: goulet salmon b. Nat Genet. 2003 Apr;33(4):463-5. doi: 10.1038/ng1122. Epub 2003 Mar 10. Nat Genet. 2003. PMID: 12627230
Pseudotumor cerebri associated with Sjögren's syndrome.
Stanescu D, Bodaghi B, Huong DL, Milea D, Goulet-Salmon B, Piette JC, LeHoang P. Stanescu D, et al. Among authors: goulet salmon b. Graefes Arch Clin Exp Ophthalmol. 2003 Apr;241(4):339-42. doi: 10.1007/s00417-002-0620-6. Epub 2003 Mar 15. Graefes Arch Clin Exp Ophthalmol. 2003. PMID: 12719998