Fukushima Yoshimitsu | Department Of Human Genetics Shinshu University School Of Medicine

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概要

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著作論文

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
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
Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome
Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB
Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis : Identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies
Sequelae of Sarin Toxicity at One and Three Years After Exposure in Matsumoto, Japan
Progressive Scoliosis in Cri-Du-Chat Syndrome Over a 20-Year Follow-Up Period : A Case Report
Discordance Between the Morphological and Physiological Information of 64-Slice MSCT Coronary Angiography and Myocardial Perfusion Imaging in Patients With Intermediate to High Probability of Coronary Artery Disease
Pitfalls of chromosome analysis
Breakpoint determination of X;autosome balanced translocations in four patients with premature ovarian failure
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
Molecular karyotyping in 17 patients and mutation screening in 41 patients with Kabuki syndrome
Cerebral hemorrhage in Fabry's disease

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