スポンサーリンク
Department Of Pediatrics Hokkaido University Graduate School Of Medicine | 論文
- A Japanese Case with Frasier Syndrome Caused by the Splice Junction Mutation of WT1 Gene
- PREDOMINANCE OF THE MUTATION AT 1138 OF THE cDNA FOR THE FIBROBLAST GROWTH FACTOR RECEPTOR 3 IN JAPANESE PATIENTS WITH ACHONDROPLASIA
- Early diagnosis for polyarthritis of juvenile idiopathic arthritis using systemic gallium scintigraphy
- TCOF1遺伝子における新奇のサイレント欠損、ミスセンス変異、ナンセンス変異の検出
- A Japanese Patient of Congenital Hypothyroidism with Cerebellar Atrophy
- Induction of IgE synthesis by genetically modified CD8+ T cells of a patient with adenosine deaminase deficiency
- Possible involvement of the tip of temporal lobe in Landau-Kleffner syndrome
- An infantile/juvenile form of Alexander disease caused by a R79H mutation in GFAP
- Application of Magnetoencephalography in Epilepsy Patients with Widespread Spike or Slow-wave Activity
- Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome
- Comparison of two assays for fibroblast growth factor (FGF)-23
- A novel splicing mutation of the ATRX gene in ATR-X syndrome
- A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)
- Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
- Elevated serum levels of soluble interleukin-2 receptor in juvenile dermatomyositis
- Experimental Investigation of the ^Zr(p,t)^Zr Reaction at 51.7 MeV
- ^Zr(p, t)^Zr Reaction at 51.7 MeV
- Photoproton Spectrum from ^V
- Photoproton Spectra from Natural Sulphur
- Photoproton Spectra from Sulphur