TY  - JOUR 
AU  - Castillejo, A
AU  - Guarinos, C
AU  - Martínez-Canto, A
AU  - Barbera VM
AU  - Egoavil C
AU  - Castillejo MI
AU  - Perez-Carbonell, L
AU  - Sanchez-Heras, AB
AU  - Segura, A
AU  - Ochoa, E
AU  - Lázaro, R
AU  - Ruiz Ponte, Clara
AU  - Bujanda, L
AU  - Andreu, M
AU  - Castells, A
AU  - Carracedo Álvarez, Ángel
AU  - Llor, X
AU  - Clofent, J
AU  - Alenda, C
AU  - Paya, A
AU  - Jover, R
AU  - Soto, JL
PY  - 2011
SN  - 1471-2350
UR  - http://hdl.handle.net/20.500.11940/6712
AB  - BACKGROUND:
Lynch syndrome (LS) is an autosomal dominant inherited cancer syndrome characterized by early onset cancers of the colorectum, endometrium and other tumours. A significant proportion of DNA variants in LS patients are unclassified....
LA  - eng
KW  - Signal Transducing
KW  - Case-Control Studies
KW  - Colorectal Neoplasms
KW  - Colorectal Neoplasms Hereditary Nonpolyposis
KW  - Family
KW  - Genotype
KW  - Humans
KW  - Microsatellite Instability
KW  - MutL Protein Homolog 1
KW  - Mutation
KW  - Nuclear Proteins/genetics
TI  - Evidence for classification of c.1852_1853AA>GC in MLH1 as a neutral variant for Lynch syndrome
DO  - 10.1186/1471-2350-12-12
T2  - BMC Medical Genetics
VL  - 12
ER  -