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Clinical characteristics of Polish patients with molecularly confirmed Mowat -Wilson syndrome | Journal of Applied Genetics
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HELP HIM REACH HIS NEXT STEP – GOAL R 10 000 - Click 'n Donate, Fundraising South Africa, for South Africans
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Figure 1 from Case Report Mowat-Wilson syndrome: clinical and molecular report of the first case in mainland China | Semantic Scholar
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Frontiers | Three Novel De Novo ZEB2 Variants Identified in Three Unrelated Chinese Patients With Mowat-Wilson Syndrome and A Systematic Review
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Mowat-Wilson Syndrome, clinical features of Patients 3 and 4 at age:... | Download Scientific Diagram
Faces of Mowat-Wilson Syndrome - 2018 | Today we honor all families affected by Mowat-Wilson Syndrome and other rare diseases. Up your volume and enjoy the most beautiful children! Songs by Leo...
Jessica_Rakshys on X: "Together We Give. #GivingTuesday is an opportunity for people around the world to stand together in unity — let's rally and support the Mowat-Wilson Syndrom Foundation to help fund
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ZEB2 Gene Mutation and Duplication of 22q11.23 in Mowat-Wilson Syndrome - Ersida Buraniqi, Manikum Moodley, 2015
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