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1 Ergebnisse
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Loss-of-function mutations in FGFR1 cause autosomal dominan..:
Dodé, Catherine
;
Levilliers, Jacqueline
;
Dupont, Jean-Michel
...
Nature Genetics. 33 (2003) 4 - p. 463-465 , 2003
Link:
https://doi.org/10.1038/ng1122
RT Journal T1
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1038_ng1122&Exemplar=1&LAN=DE A1 Dodé, Catherine A1 Levilliers, Jacqueline A1 Dupont, Jean-Michel A1 De Paepe, Anne A1 Le Dû, Nathalie A1 Soussi-Yanicostas, Nadia A1 Coimbra, Roney S. A1 Delmaghani, Sedigheh A1 Compain-Nouaille, Sylvie A1 Baverel, Françoise A1 Pêcheux, Christophe A1 Le Tessier, Dominique A1 Cruaud, Corinne A1 Delpech, Marc A1 Speleman, Frank A1 Vermeulen, Stefan A1 Amalfitano, Andrea A1 Bachelot, Yvan A1 Bouchard, Philippe A1 Cabrol, Sylvie A1 Carel, Jean-Claude A1 Delemarre-van de Waal, Henriette A1 Goulet-Salmon, Barbara A1 Kottler, Marie-Laure A1 Richard, Odile A1 Sanchez-Franco, Franco A1 Saura, Robert A1 Young, Jacques A1 Petit, Christine A1 Hardelin, Jean-Pierre PB Springer Science and Business Media LLC YR 2003 SN 1061-4036 SN 1546-1718 JF Nature Genetics VO 33 IS 4 SP 463 OP 465 LK http://dx.doi.org/https://doi.org/10.1038/ng1122 DO https://doi.org/10.1038/ng1122 SF ELIB - SuUB Bremen
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