Matches in DBpedia 2015-10 for { <http://doi.org/10.1007/s10038-006-0010-8> ?p ?o }
Showing triples 1 to 22 of
22
with 100 triples per page.
- s10038-006-0010-8 author1 "Koolen, D. A.".
- s10038-006-0010-8 author10 "de Vries, B. B. A.".
- s10038-006-0010-8 author2 "Herbergs, J.".
- s10038-006-0010-8 author3 "Veltman, J. A.".
- s10038-006-0010-8 author4 "Pfundt, R.".
- s10038-006-0010-8 author5 "van Bokhoven, H.".
- s10038-006-0010-8 author6 "Stroink, H.".
- s10038-006-0010-8 author7 "Sistermans, E. A.".
- s10038-006-0010-8 author8 "Brunner, H. G.".
- s10038-006-0010-8 author9 "Geurts van Kessel, A.".
- s10038-006-0010-8 doi "10.1007/s10038-006-0010-8".
- s10038-006-0010-8 isCitedBy FBXW11.
- s10038-006-0010-8 isCitedBy Young–Madders_syndrome.
- s10038-006-0010-8 issue "8".
- s10038-006-0010-8 journal "Journal of Human Genetics".
- s10038-006-0010-8 pages "721–6".
- s10038-006-0010-8 pages "721–726".
- s10038-006-0010-8 pmid "16865294".
- s10038-006-0010-8 title "Holoprosencephaly and preaxial polydactyly associated with a 1.24 Mb duplication encompassing FBXW11 at 5q35.1".
- s10038-006-0010-8 vauthors "Koolen DA, Herbergs J, Veltman JA, Pfundt R, van Bokhoven H, Stroink H, Sistermans EA, Brunner HG, Geurts van Kessel A, de Vries BB".
- s10038-006-0010-8 volume "51".
- s10038-006-0010-8 year "2006".