スポンサーリンク
Department of Human Genetics, Radboud University Nijmegen Medical Centre | 論文
- Holoprosencephaly and preaxial polydactyly associated with a 1.24Mb duplication encompassing FBXW11 at 5q35.1
- Long-term follow-up of patients with recessive dystrophic epidermolysis bullosa in the Netherlands : Expansion of the mutation database and unusual phenotype-genotype correlations