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Department Of Baioscience And Biotechnology Shinshu University | 論文
- 168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
- 186 TYROID DYSFUNCTION IN VERY-LOW-BIRTH-WEIGHT-INFANTS
- 96 A ONE-MONTH-OLD FEMALE NEONATE CASE OF NONCLASSICAL STEROID 21-HYDROXYLASE DEFICIENCY DIAGNOSED BY MOLECULAR ANALYSIS OF THE CYP21 GENE.
- 204 A CASE OF CHROMOSOME BREAKAGE SYNDROME WITH SEVERE GROWTH FAILURE AND SYSTEMIC BONE DISEASE