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Results: 2

Authors: van Bokhoven, H Celli, J Kayserili, H van Beusekom, E Balci, S Brussel, W Skovby, F Kerr, B Percin, EF Akarsu, N Brunner, HG
Citation: H. Van Bokhoven et al., Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome, NAT GENET, 25(4), 2000, pp. 423-426

Authors: Zguricas, J Heus, H Morales-Peralta, E Breedveld, G Kuyt, B Mumcu, EF Bakker, W Akarsu, N Kay, SPJ Hovius, SER Heredero-Baute, L Oostra, BA Heutink, P
Citation: J. Zguricas et al., Clinical and genetic studies on 12 preaxial polydactyly families and refinement of the localisation of the gene responsible to a 1.9 cM region on chromosome 7q36, J MED GENET, 36(1), 1999, pp. 32-40
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