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John Wiley & Sons Inc

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Identification of ABCC6 pseudogenes on human chromosome 16p: implications for mutation detection in pseudoxanthoma elasticum

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Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

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Mapping of Both Autosomal Recessive and Dominant Variants of Pseudoxanthoma Elasticum to Chromosome 16p13.1

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