Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome-Reference-Cited by-同舟云学术

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Published:2003-03-10 Issue:4 Volume:33 Page:463-465
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Dodé Catherine,Levilliers Jacqueline,Dupont Jean-Michel,De Paepe Anne,Le Dû Nathalie,Soussi-Yanicostas Nadia,Coimbra Roney S.,Delmaghani Sedigheh,Compain-Nouaille Sylvie,Baverel Françoise,Pêcheux Christophe,Le Tessier Dominique,Cruaud Corinne,Delpech Marc,Speleman Frank,Vermeulen Stefan,Amalfitano Andrea,Bachelot Yvan,Bouchard Philippe,Cabrol Sylvie,Carel Jean-Claude,Delemarre-van de Waal Henriette,Goulet-Salmon Barbara,Kottler Marie-Laure,Richard Odile,Sanchez-Franco Franco,Saura Robert,Young Jacques,Petit Christine,Hardelin Jean-Pierre

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1122.pdf

Reference15 articles.

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3. White, B.J., Rogol, A.D., Brown, K.S., Lieblich, J.M. & Rosen, S.W. Am. J. Med. Genet. 15, 417–436 (1983).

4. Oliveira, L.M.B. et al. J. Clin. Endocrinol. Metab. 86, 1532–1538 (2001).

5. Vermeulen, S. et al. Am. J. Med. Genet. 108, 315–318 (2002).

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