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Results: 1-2 |
Results: 2
Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux
Authors: Bartels, Cynthia F. Bükülmez, Hülya Padayatti, Pius Rhee, David K. Ravenswaaij-Arts, Conny, Van Pauli, Richard M. Mundlos, Stefan Chiatayat, David Shih, Ling-Yu Al-Gazali, Lihadh I. Kant, Sarina Cole, Trevor Morton, Jenny Cormier-Daire, Valérie Faivre, Laurence Lees, Melissa Kirk, Jeremy Mortier, Geert R. Leory, Jules Zabel, Bernhard Kim, Chong Ae Crow, Yanick Braveman, Nancy E. Akker, Focco, Van : der Warman, Matthew L.
Citation: F. Bartels, Cynthia et al., Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux, American journal of human genetics , 75(1), 2004, pp. 27-34
Association of congenital deficiency of multiple vitamin k-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives
Authors: Pauli, Richard M. Lian, Jane B. Mosher, Deane F. Suttie, John W.
Citation: M. Pauli, Richard et al., Association of congenital deficiency of multiple vitamin k-dependent coagulation factors and the phenotype of the warfarin embryopathy: clues to the mechanism of teratogenicity of coumarin derivatives, American journal of human genetics , 41-II(4), 1987, pp. 566-583
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