Kofod Mack

  • Kofod Mack heeft een update geplaatst 1 week, 4 dagen geleden

    The remaining 20 variants have not been documented to date. In one patient, we detected a large deletion including the entire FBN1 gene using the array CGH approach. Currently, there are very few studies on the genotype-phenotype correlation of patients with MFS, and no clear genotype-phenotype maps for MFS have been constructed so far, except for…[Lees meer]

  • Kofod Mack is geregistreerd lid geworden 1 week, 4 dagen geleden

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