スポンサーリンク
Department Of Pediatrics Nagasaki University Graduate School Of Biomedical Sciences | 論文
- LRP5, low-density-lipoprotein-receptor-related protein 5, is a determinant for bone mineral density
- On the conflicting reports of imprinting status of mouse ATPIOa in the adult brain : strain-background-dependent imprinting?
- Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophy
- Protein-losing enteropathy complicated with recurrent convulsions and developmental delay in a 4-month-old boy
- Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family
- A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet
- Nonaka myopathy is caused by mutations in the UDP-N-acetylglucosamine-2-epimerase/N-acetylmannosamine kinase gene (GNE)
- A 1.5-Mb PAC/BAC Contig Spanning the Prader-Willi Syndrome Critical Region (PWCR)
- Genetic Counseling System in Nagasaki University Hospital and Genetic Services in Nagasaki Prefecture-Now and Future
- Special Report A Genetic Counseling System in Nagasaki Prefecture: The Course and Current Status of the Genetic Counseling Unit in Nagasaki University Hospital
- Differential T-cell response in a young child and neonates with toxic shock syndrome
- 243 A CASE OF McCUNE-ALBRIGHT SYNDROME WITH NARROWING OPTIC CANAL : A TRIAL OF INTRAVENOUS PAMIDRONATE TREATMENT
- Pediatric CT scan usage in Japan : results of a hospital survey
- Osteogenic Action of Parathyroid Hormone-Related Peptide (1-141) in Rat ROS Cells
- Establishment and Characterization of a Malignant Epithelioid Hemangioendothelioma from Mouse Thyroid Tumor
- A Case of Basal Cell Adenocarcinoma of the Parotid Gland
- A Case of Leiomyosarcoma of the Sphenoid Sinus
- Review Article Children with Chronic Granulomatous Disease
- A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy
- A case of megalocornea-mental retardation syndrome complicated with bilateral sensorineural hearing impairment