スポンサーリンク
Medical Genetics, Department of Molecular Biology, University of Siena | 論文
- Clinical and molecular characterization of Italian patients affected by Cohen syndrome
- Array comparative genomic hybridization in retinoma and retinoblastoma tissues
- Leukoencephalopathy in 21-β hydroxylase deficiency : Report of a family
- Mutational screening of the RB1 gene in Italian patients with retinoblastoma reveals 11 novel mutations
- A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita