Showing results 1 to 7 of 7
Title | Author(s) | Issue Date | |
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2016 | |||
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2 Journal:Human Molecular Genetics | 2010 | ||
Genome-wide copy number variation study in anorectal malformations Journal:Human Molecular Genetics | 2013 | ||
Mutations in the NRG1 gene are associated with Hirschsprung disease Journal:Human Genetics | 2012 | ||
Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis Journal:BMC Medical Genomics | 2017 | ||
2011 | |||
Sacral agenesis: a pilot whole exome sequencing and copy number study Journal:BMC Medical Genetics | 2016 |