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- W2016823672 abstract "A case of oculocerebrorenal (Löwe) syndrome is presented in which analysis of the pattern of RFLP suggested that the gene originally mutated in the grandfather' s X-chromosome and became clinically apparent in one of his male grandsons." @default.
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- W2016823672 date "1990-04-01" @default.
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- W2016823672 title "Prenatal diagnosis of Löwe'S syndrome: A case report with evidence ofde novo mutation" @default.
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- W2016823672 doi "https://doi.org/10.1002/pd.1970100408" @default.
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