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A missense mutation in the ZFHX1B gene associated with an atypical Mowat– Wilson syndrome phenotype - Heinritz - 2006 - American Journal of Medical Genetics Part A - Wiley Online Library
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Facial appearance of Mowat-Wilson syndrome patients. (A) Patient 1 (age... | Download Scientific Diagram
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Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care | Genetics in Medicine
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