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- 2023
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Mark
Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy
(
- Contribution to journal › Article
- 2022
-
Mark
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
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- Contribution to journal › Article
- 2020
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Mark
SLC20A1 Is Involved in Urinary Tract and Urorectal Development
(
- Contribution to journal › Article
- 2019
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Mark
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene
(
- Contribution to journal › Article
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Mark
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
(
- Contribution to journal › Article