スポンサーリンク
Department of Pediatrics, Asahikawa Medical Collage | 論文
- Association of SLC6A9 Gene Variants with Human Essential Hypertension
- 43 Common origin of the Q258X mutation in StAR gene responsible for congenital aderenal lipoid hyperplasia in Japanese
- A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions
- Haplotype analysis of the human collectin placenta 1 (hCL-P1) gene
- Linkage and association analyses of the osteoprotegerin gene locus with human osteoporosis
- Acute disseminated encephalomyelitis in an infant with incontinentia pigmenti
- L1CAM mutation in a Japanese family with x-linked hydrocephalus: a study for genetic counseling
- The role of different X-inactivation pattern on the variable clinical phenotype with Rett syndrome
- Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
- 161 A NOVEL MUTATION IN SOX9 GENE IN A CASE OF CAMPOMELIC DYSPLASIA