Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.

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Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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Common genetic variants in GAL ...... ility to Hirschsprung disease.

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P1476

Common genetic variants in GAL ...... bility to Hirschsprung disease

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P2093

Beilin Gu

http://www.w3.org/2001/XMLSchema#string

Jie Chen

http://www.w3.org/2001/XMLSchema#string

Jun Wang

http://www.w3.org/2001/XMLSchema#string

Wei Cai

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Weihui Yan

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Ying Zhou

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P2860

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

PLINK: a tool set for whole-genome association and population-based linkage analyses

Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model

MASH1/Ascl1a leads to GAP43 expression and axon regeneration in the adult CNS

Galanin and the neuroendocrine axes

G*Power 3: a flexible statistical power analysis program for the social, behavioral, and biomedical sciences

Controlling the false discovery rate in behavior genetics research

Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability

Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations.

Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.

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3377-3387

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scholarly article

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10.1111/JCMM.13612

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P433

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P478

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Yang Wang

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2018-04-14T00:00:00Z

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P698

29654647

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6010875

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