スポンサーリンク
Department of Medical Genetics, Shinshu University School of Medicine | 論文
- The IHPK1 gene is disrupted at the 3p21. 31 breakpoint of t(3 ; 9) in a family with type 2 diabetes mellitus
- Molecular characterization of a novel translocation t(5 ; 14)(q21 ; q32) in a patient with congenital abnormalities
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- OJ-256 Incremental Diagnostic Value of Fusion Imaging from Stress Myocardial Scintigraphy and Coronary Multi-slice CT(OJ43,Nuclear Cardiology (Coronary, Myocardium) (I),Oral Presentation (Japanese),The 73rd Annual Scientific Meeting of The Japanese Circul
- Usefulness of ^TlCl/^I-BMIPP dual-myocardial SPECT for patients with non-ST segment elevation myocardial infarction
- A novel gene is disrupted at a 14q13 breakpoint of t(2;14) in a patient with mirror-image polydactyly of hands and feet
- Guidelines for genetic testing
- Familial 14-Mb deletion at 21q11.2-q21.3 and variable phenotypic expression
- A novel splicing mutation of the ATRX gene in ATR-X syndrome
- The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32
- Serial assessment of left ventricular performance at rest and during bicycle exercise by ECG-gated myocardial perfusion SPECT
- Unusual Clinical and Pathological Presentation of a Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1
- Less Frequent NSD1-Intragenic Deletions in Japanese Sotos Syndrome: Analysis of 30 Patients by NSD1-Exon Array CGH, Quantitative Fluorescent Duplex PCR, and Fluorescence In Situ Hybridization
- Assessment of contractile response to dobutamine stress by means of ECG-gated myocardial SPECT : Comparison with myocardial perfusion and fatty acid metabolism
- Assessment of left ventricular function using solid-state gamma camera equipped with a highly-sensitive collimator
- Assessment of myocardial washout of Tc-99m-sestamibi in patients with chronic heart failure : Comparison with normal control
- Long-term Follow-up of Patients with Multiple Endocrine Neoplasia Type 1
- Validation of fast-RAMLA in clinical PET
- Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1
- Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan