Co‐occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

BACKGROUND: Lynch syndrome (LS) is a hereditary condition characterized by a high risk of colorectal cancer, endometrial cancer, and other neoplasia associated with germline alterations in DNA mismatch repair genes. The classical genetic diagnostic strategy for LS consists of the Sanger sequencing o...

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Detalles Bibliográficos
Autores principales: Ferrer‐Avargues, Rosario, Castillejo, María Isabel, Dámaso, Estela, Díez‐Obrero, Virginia, Garrigos, Noemí, Molina, Tatiana, Codoñer‐Alejos, Alan, Segura, Ángel, Sánchez‐Heras, Ana Beatriz, Castillejo, Adela, Soto, José Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968885/
https://www.ncbi.nlm.nih.gov/pubmed/33630411
http://dx.doi.org/10.1002/cac2.12134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7968885/
https://www.ncbi.nlm.nih.gov/pubmed/33630411
http://dx.doi.org/10.1002/cac2.12134

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