Mizuno Seiji | Department Of Pediatrics Central Hospital Aichi Human Service Center

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著作論文

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

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