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Nature Publishing Group | 論文
- Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss
- Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia
- Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder
- The era of genome-wide association studies : opportunities and challenges for asthma genetics
- Prediction of the clinical phenotype of Fabry disease based on protein sequential and structural information
- Familiar Meniere's disease restricted to 1.48Mb on chromosome 12p12.3 by allelic and haplotype association
- MEFV mutation carriage in Israeli Jewish individuals from ethnicities with low risk for familial Mediterranean fever
- A hard road in psychiatric genetics : schizophrenia and DPYSL2
- No influence of FAT polymorphisms in response to aripiprazole
- Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian family
- Adrenergic-β2 receptor polymorphism and athletic performance
- Association study between single-nucleotide polymorphisms in 199 drug-related genes and commonly measured quantitative traits of 752 healthy Japanese subjects
- Diagnosis and fine mapping of a deletion in distal 11q in two Chinese patients with developmental delay
- Implications of gene copy-number variation in health and diseases
- Association of LOXL1 gene with Finnish exfoliation syndrome patients
- Selective neutrality analysis of 17 STRs in Mediterranean populations
- Association of the leptin gene with knee osteoarthritis susceptibility in a Han Chinese population : a case-control study
- The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility
- A case-control association analysis of CABIN1 with schizophrenia in a Japanese population
- Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations