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Prenatal presentation of Walker–Warburg syndrome with a POMT2 mutation: an extended fetal phenotype | Egyptian Journal of Medical Human Genetics | Full Text
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160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker–Warburg syndrome - ScienceDirect
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Brain and Eye Malformations Resembling Walker–Warburg Syndrome Are Recapitulated in Mice by Dystroglycan Deletion in the Epiblast | Journal of Neuroscience
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POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome | Journal of Medical Genetics
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Walker-Warburg Syndrome - Journal of American Association for Pediatric Ophthalmology and Strabismus {JAAPOS}
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SciELO - Brasil - Walker-Warburg syndrome: report of two cases Walker-Warburg syndrome: report of two cases
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