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Michel Syndrome (oculopalatoskeletal syndrome)

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Encyclopedia of Genetics, Genomics, Proteomics and Informatics
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An autosomal recessive multiple defect involving the eyelid, opacity of the cornea, cleft lip and palate, defects of the inner ear and spine column, etc. It causes complete deafness. deafness, eye diseases

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(2008). Michel Syndrome (oculopalatoskeletal syndrome). In: Encyclopedia of Genetics, Genomics, Proteomics and Informatics. Springer, Dordrecht. https://doi.org/10.1007/978-1-4020-6754-9_10318

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