Genomic copy number variation analysis in multiple system atrophy.

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Genomic copy number variation analysis in multiple system atrophy.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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Genomic copy number variation analysis in multiple system atrophy.

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Genomic copy number variation analysis in multiple system atrophy.

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Genomic copy number variation analysis in multiple system atrophy.

@en

Genomic copy number variation analysis in multiple system atrophy.

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Genomic copy number variation analysis in multiple system atrophy.

@en

Genomic copy number variation analysis in multiple system atrophy.

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P1476

Genomic copy number variation analysis in multiple system atrophy

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P2093

Ichigaku Takigawa

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Ichiro Yabe

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Ikuko Takahashi

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Jun Utsumi

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Masaaki Matsushima

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Masataka Katsu

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Takayuki Katayama

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Yuka Hama

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P2860

Initial sequencing and analysis of the human genome

Copy number loss of (src homology 2 domain containing)-transforming protein 2 (SHC2) gene: discordant loss in monozygotic twins and frequent loss in patients with multiple system atrophy

The Sequence of the Human Genome

Structural variation in the human genome

Finding the missing heritability of complex diseases

Rare chromosomal deletions and duplications increase risk of schizophrenia

Multiple system atrophy: cellular and molecular pathology.

Prader-Willi syndrome is caused by disruption of the SNRPN gene

The impact of retrotransposons on human genome evolution

Strong association of de novo copy number mutations with autism

P2888

s13041-017-0335-6

P304

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P31

scholarly article

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10.1186/S13041-017-0335-6

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P433

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P478

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Hidenao Sasaki

P577

2017-11-29T00:00:00Z

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P6179

1093054984

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29187220

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5708077

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