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