Cargando…
A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory
Lynch syndrome (LS) is caused by mutations in mismatch repair genes and is characterized by a high cumulative risk for the development of mainly colorectal carcinoma and endometrial carcinoma. Early detection of LS is important since surveillance can reduce morbidity and mortality. However, the diag...
Autores principales: | Van Lier, Margot GF, Wagner, Anja, Van Leerdam, Monique E, Biermann, Katharina, Kuipers, Ernst J, Steyerberg, Ewout W, Dubbink, Hendrikus Jan, Dinjens, Winand NM |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3837620/ https://www.ncbi.nlm.nih.gov/pubmed/19929944 http://dx.doi.org/10.1111/j.1582-4934.2009.00977.x |
Ejemplares similares
-
Gynecological Surveillance and Surgery Outcomes in Dutch Lynch Syndrome Carriers
por: Eikenboom, Ellis L., et al.
Publicado: (2021) -
Novel EGFR V834L Germline Mutation Associated With Familial Lung Adenocarcinoma
por: van der Leest, Cor, et al.
Publicado: (2018) -
Somatic mosaicism by a de novo MLH1 mutation as a cause of Lynch syndrome
por: Geurts‐Giele, Willemina R., et al.
Publicado: (2019) -
“The leading role of pathology in assessing the somatic molecular alterations of cancer: Position Paper of the European Society of Pathology”: letter to the Editor
por: Dinjens, Winand N. M., et al.
Publicado: (2020) -
Genetic testing for Lynch syndrome: family communication and motivation
por: Leenen, Celine H. M., et al.
Publicado: (2015)