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2022
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2011
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X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.
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S-EPMC3374620
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biostudies-literature
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Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
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S-EPMC9132874
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biostudies-literature
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