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Results: 2

Authors: Nurnberg, P Thiele, H Chandler, D Hohne, W Cunningham, ML Ritter, H Leschik, G Uhlmann, K Mischung, C Harrop, K Goldblatt, J Borochowitz, ZU Kotzot, D Westermann, F Mundlos, S Braun, HS Laing, N Tinschert, S
Citation: P. Nurnberg et al., Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia, NAT GENET, 28(1), 2001, pp. 37-41

Authors: Lambiris, N Peters, H Bollmann, R Leschik, G Leisti, J Salonen, R Cobet, G Oostra, BA Willemsen, R
Citation: N. Lambiris et al., Rapid FMR1-protein analysis of fetal blood: an enhancement of prenatal diagnostics, HUM GENET, 105(3), 1999, pp. 258-260
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