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
- Successful treatment with rituximab of refractory idiopathic thrombocytopenic purpura in a patient with Kabuki syndrome
- Evolution of seizures and electroencephalographical findings in 23 cases of deletion type Angelman syndrome
- Static and Dynamical Properties of SH Phonons Related to Resonant Tansmission through Double-Barrier Structure
- Caffeine yields aneuploidy through asymmetrical cell division caused by misalignment of chromosomes
- Multiple-Barrier Systems for Phonons: Transmission Characteristics
- 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
- Time Advance and Delay of Phonon Packets Scattered off Superlattice Systems
- 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