TY  - JOUR
AU  - Picó, María Dolores
AU  - Castillejo, Adela
AU  - Murcia, Óscar
AU  - Giner-Calabuig, Mar
AU  - Alustiza, Miren
AU  - Sánchez, Ariadna
AU  - Moreira, Leticia
AU  - Pellise, María
AU  - Castells, Antoni
AU  - Carrillo-Palau, Marta
AU  - Ramon Y Cajal, Teresa
AU  - Gisbert-Beamud, Alexandra
AU  - Llort, Gemma
AU  - Yagüe, Carmen
AU  - López-Fernández, Adriá
AU  - Alvarez-Urturi, Cristina
AU  - Cubiella, Joaquin
AU  - Rivas, Laura
AU  - Rodríguez-Alcalde, Daniel
AU  - Herraiz, Maite
AU  - Garau, Catalina
AU  - Dolz, Carlos
AU  - Bujanda, Luis
AU  - Cid, Lucia
AU  - Povés, Carmen
AU  - Garzon, Marta
AU  - Salces, Inmaculada
AU  - Ponce, Marta
AU  - Hernández-Villalba, Luís
AU  - Alenda, Cristina
AU  - Balaguer, Francesc
AU  - Soto, Jose-Luis
AU  - Jover, Rodrigo
PY  - 2019
DO  - 10.1016/j.cgh.2019.06.012
UR  - http://hdl.handle.net/10668/14151
T2  - Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
AB  - Lynch syndrome is characterized by DNA mismatch repair (MMR) deficiency. Some patients with suspected Lynch syndrome have DNA MMR deficiencies but no detectable mutations in genes that encode MMR proteins-this is called Lynch-like syndrome (LLS)....
LA  - en
KW  - Colon Tumor
KW  - Familial
KW  - Genetic
KW  - Polyp
KW  - Risk
KW  - Colorectal Neoplasms
KW  - Colorectal Neoplasms, Hereditary Nonpolyposis
KW  - DNA Mismatch Repair
KW  - Female
KW  - Humans
KW  - Microsatellite Instability
KW  - MutL Protein Homolog 1
KW  - Neoplastic Syndromes, Hereditary
TI  - Clinical and Pathological Characterization of Lynch-Like Syndrome.
TY  - research article
VL  - 18
ER  -