A novel germline MLH1 mutation causing Lynch Syndrome in patients from the Republic of Macedonia

AIM: To implement molecular analysis in the clinical diagnosis and management of Lynch syndrome (LS). METHODS: We analyzed the mutations in MLH1 and MSH2 in the selected LS families from the Republic of Macedonia. RESULTS: We performed the very first genetic identification of LS families and charact...

Descripción completa

Detalles Bibliográficos
Autores principales: Hiljadnikova-Bajro, Marija, Josifovski, Toni, Panovski, Milco, Dimovski, Aleksandar J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Medical Schools 2012
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490460/
https://www.ncbi.nlm.nih.gov/pubmed/23100212
http://dx.doi.org/10.3325/cmj.2012.53.496

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3490460/
https://www.ncbi.nlm.nih.gov/pubmed/23100212
http://dx.doi.org/10.3325/cmj.2012.53.496

Ejemplares similares