Showing results 1 to 7 of 7
Title | Author(s) | Issue Date | |
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2010 | |||
Fine mapping of the NRG1 hirschsprung's disease locus Journal:PLoS ONE | 2011 | ||
Genome-wide copy number variation study in anorectal malformations Journal:Human Molecular Genetics | 2013 | ||
Hedgehog/notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans Journal:Journal of Clinical Investigation | 2011 | ||
A hierarchical frailty model applied to two-generation melanoma data Journal:Lifetime Data Analysis | 2010 | ||
2021 | |||
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese Journal:Human Molecular Genetics | 2012 |