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Proceedings: Pseudo-rubinstein syndrome: an autosomal dominant condition

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ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.

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Identification of the Novel HLA-DRB1*11:01:49 Allele Using Next-Generation Sequencing in a Chinese Individual.

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Proceedings: Pseudo-rubinstein syndrome: an autosomal dominant condition

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