スポンサーリンク
Department Of Pediatrics Central Hospital Aichi Human Service Center | 論文
- Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome
- Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
- Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome
- Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
- Clinical variability in a Japanese hereditary lymphedema type I family with an FLT4 mutation
- Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
- HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
- Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies