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rh-mod syndrome
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RHAG
Identification of 5' flanking sequence of RH50 gene and the core region for erythroid-specific expression
Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment
Rh-deficiency of the regulator type caused by splicing mutations in the human RH50 gene
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