スポンサーリンク
Sapporo City Institute of Public Health | 論文
- Hemolytic crisis with fulminant hepatic failure in Wilson disease without consanguinity
- Screening for the Mutations in Mitochondrial DNA Predisposed to Hearing Loss Using Noninvasive Samples
- Mutations of the CYP21 Gene in Nonclassical Steroid 21-Hydroxylase Deficiency in Japan
- Prenatal Diagnosis of Steroid 21-Hydroxylase Deficiency by the Modified Polymerase Chain Reaction to Detect Splice Site Mutation in the CYP21 Gene
- 34 NOVEL MUTATIONS IN THE CYP11B1 GENE IN JAPANESEPATIENTS WITH CONGENITAL ADRENAL HYPERPLASIA DUE TO 11β-HYDROXYIASE DEFICIENCY
- Effects of Dioxins and Polychlorinated Biphenyls (PCBs) on Thyroid Function in Infants Born in Japan : Report from Research on Environmental Health
- Prenatal diagnosis of the Wiskott-Aldrich syndrome by PCR-based methods
- 34 THIAMAZOL OR PROPILTHIOURACIL AND L-T4 COMBINATION THERAPY FOR INFANTS BORN TO MOTHER WITH GRAVES' DISEASE
- 100 ANALYSIS OF CYP21 GENE IN STEROID 21-HYDROXYLASE DEFICIENCY IN HIROSHIMA PREFECTURE