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Results:
1-3
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Results: 3
Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7
Authors:
Hehr, U Dorr, S Hagemann, M Hansmann, I Preiss, U Bromme, S
Citation:
U. Hehr et al., Silver-Russell syndrome and cystic fibrosis associated with maternal uniparental disomy 7, AM J MED G, 91(3), 2000, pp. 237-239
Craniosynostosis syndromes: From genes to premature fusion of skull bones
Authors:
Hehr, U Muenke, M
Citation:
U. Hehr et M. Muenke, Craniosynostosis syndromes: From genes to premature fusion of skull bones, MOL GEN MET, 68(2), 1999, pp. 139-151
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
Authors:
Wallis, DE Roessler, E Hehr, U Nanni, L Wiltshire, T Richieri-Costa, A Gillessen-Kaesbach, G Zackai, EH Rommens, J Muenke, M
Citation:
De. Wallis et al., Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly, NAT GENET, 22(2), 1999, pp. 196-198
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