| scholarly article | Q13442814 |
| P356 | DOI | 10.1097/MPG.0B013E3181FF2E5B |
| P698 | PubMed publication ID | 21336163 |
| P2093 | author name string | Randolph P Matthews | |
| Pierre Russo | |||
| Shuang Cui | |||
| Barbara A Haber | |||
| Jessi Erlichman | |||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Mowat-Wilson syndrome | Q2757585 |
| P304 | page(s) | 339-344 | |
| P577 | publication date | 2011-03-01 | |
| P1433 | published in | Journal of Pediatric Gastroenterology and Nutrition | Q6295721 |
| P1476 | title | Intrahepatic biliary anomalies in a patient with Mowat-Wilson syndrome uncover a role for the zinc finger homeobox gene zfhx1b in vertebrate biliary development | |
| P478 | volume | 52 |
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| Q89747881 | Exome Sequencing in Individuals with Isolated Biliary Atresia |
| Q38544230 | Hirschsprung's disease in children with Mowat-Wilson syndrome |
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| Q41535789 | Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish |
| Q35968743 | Methylation Microarray Studies Highlight PDGFA Expression as a Factor in Biliary Atresia |
| Q42056773 | Mutations in vacuolar H+ -ATPase subunits lead to biliary developmental defects in zebrafish. |
| Q42105636 | The Sea Lamprey as an Etiological Model for Biliary Atresia |
| Q36669372 | Zebrafish models of human liver development and disease |
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