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Phenotypic spectrum in a family with a novel RAC2 p.I21S dominant‐activating mutation
Download from doi.orgUmbilical Cord Blood Cell Clearance Post-Infusion in Immune-Competent Children with Cerebral Palsy
UploadA loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes
UploadSafety of sibling cord blood cell infusion for children with cerebral palsy
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