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; Nature Genetics, 2003, vol. 33, issue 4, p 463, ISSN 10614036. ISBN 10614036.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef