1 – 10 of 19
- show: 10
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2023
-
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
(
- Contribution to journal › Article
- 2020
-
Mark
SLC20A1 Is Involved in Urinary Tract and Urorectal Development
(
- Contribution to journal › Article
- 2019
-
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
-
Mark
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
(
- Contribution to journal › Article
- 2017
-
Mark
Self-assessed remission rates after electroconvulsive therapy of depressive disorders
(
- Contribution to journal › Article
-
Mark
ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development
(
- Contribution to journal › Article
- 2015
-
Mark
No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations.
(
- Contribution to journal › Article
-
Mark
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
(
- Contribution to journal › Article
- 2014
-
Mark
A Case with Bladder Exstrophy and Unbalanced X Chromosome Rearrangement
(
- Contribution to journal › Article