東稔 節治 | 大阪大学墓礎工学部化学工学科
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概要
論文 | ランダム
- 40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1
- 53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
- 66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome
- 64 GNAS1 mutation in a Japanese boy with progressive osseous heteroplasia.
- 98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency