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Câncer Colorretal Hereditário Sem Polipose > Publicações

Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria.

https://www.ncbi.nlm.nih.gov/pubmed/28365877
Por Juan
Pesquisador

Refining the role of PMS2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants.

https://www.ncbi.nlm.nih.gov/pubmed/23709753
Por Juan
Pesquisador