| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1002/AJMG.A.31196 |
| P698 | PubMed publication ID | 16532472 |
| P50 | author | Anita Rauch | Q21253643 |
| Denise Horn | Q56955997 | ||
| P2093 | author name string | Christiane Zweier | |
| Cornelia Kraus | |||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Mowat-Wilson syndrome | Q2757585 |
| P304 | page(s) | 869-872 | |
| P577 | publication date | 2006-04-01 | |
| P1433 | published in | American Journal of Medical Genetics | Q4744254 |
| P1476 | title | Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype. | |
| P478 | volume | 140 |
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| Q56266848 | CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases |
| Q38413219 | Clinical utility gene card for: Mowat-Wilson syndrome |
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| Q38544230 | Hirschsprung's disease in children with Mowat-Wilson syndrome |
| Q21202963 | Mowat-Wilson syndrome |
| Q31141777 | Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients |
| Q42912284 | NuRD mediates activating and repressive functions of GATA-1 and FOG-1 during blood development |
| Q47210500 | Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care |
| Q34597855 | ZFHX1B mutations in patients with Mowat-Wilson syndrome |
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