Nature Genetics
9, 108 (1995)
doi:10.1038/ng0295-108
FGFR2 mutations in Pfeiffer syndromeElisabeth Lajeunie1, Hong Wei Ma1, Jacky Bonaventure1, Arnold Munnich1, Martine Le Merrer1
& Dominique Renier2
1Unité de Recherches sur les Handicaps Génétiques de l'Enfant, INSERM U. 393, Hôpital des Enfants Malades, 149 rue de Sèvres, 75743 Paris Cedex 15, France
2Département de Neurochirurgie, Hôpital des Enfants Malades, 149 rue de Sèvres, 75743 Paris Cedex 15, France REFERENCES
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