スポンサーリンク
Department of Molecular Cytogenetics, Tokyo Medical and Dental University | 論文
- Concomitant microduplications of MECP2 and ATRX in male patients with severe mental retardation
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
- Novel deletion at Xq24 including the UBE2A gene in a patient with X-linked mental retardation