Yamamoto Kayo | Clinical Immunology Advanced Biochemical Applications Graduate School Of Comprehensive Human Sciences University Of Tsukuba
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論文 | ランダム
- Brain and behaviour in children with 22q11.2 deletion syndrome : a volumetric and voxel-based morphometry MRI study
- SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2
- COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
- 22q11.2欠失症候群
- Microduplication and triplication of 22q11.2 : a highly variable syndrome