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Dandan Ruan
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A study on the function of PH EX mutations p.Glul45* and p.Trp749Arg in families with X-linked hyphosphatemic rickets
Analysis of two pedigrees of Gitelman syndrome complicated with proteinuria or Hashimoto's thyroiditis caused by SLC12A3 compound heterozygous mutation and literature review
Mutational analysis of a familial adenomatous polyposis pedigree with bile duct polyp phenotype
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