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Journal Article
Gastroenterology, ISSN 0016-5085, 2008, Volume 135, Issue 2, pp. 419 - 428.e1
Background & Aims: Although the clinical phenotype of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer) has been well described, little... 
Gastroenterology and Hepatology | BETHESDA GUIDELINES | COLON-CANCER | DNA MISMATCH REPAIR | CHILDHOOD-CANCER | NONPOLYPOSIS COLORECTAL-CANCER | MICROSATELLITE INSTABILITY | HETEROZYGOUS MUTATIONS | GASTROENTEROLOGY & HEPATOLOGY | CONSTITUTIVE DEFICIENCY | ENDOMETRIAL CANCER | GENE PMS2 | Immunohistochemistry | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | DNA Repair Enzymes - genetics | Gene Expression Regulation, Neoplastic | Colorectal Neoplasms - chemistry | DNA-Binding Proteins - analysis | Male | DNA Mutational Analysis - methods | Endometrial Neoplasms - genetics | Ligase Chain Reaction | Adenosine Triphosphatases - analysis | Polymerase Chain Reaction | Germ-Line Mutation | Adult | Female | Mismatch Repair Endonuclease PMS2 | Odds Ratio | Endometrial Neoplasms - chemistry | Risk Assessment | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Genotype | Penetrance | DNA-Binding Proteins - genetics | DNA Repair Enzymes - analysis | Phenotype | Proto-Oncogene Proteins B-raf - genetics | Endometrial Neoplasms - pathology | Heterozygote | Adenosine Triphosphatases - genetics | Aged | Colorectal Neoplasms, Hereditary Nonpolyposis - chemistry | Colorectal Neoplasms - pathology | Genetic aspects | Research | Oncology, Experimental | Colorectal cancer | Cancer | Index Medicus | Abridged Index Medicus
Journal Article
Familial Cancer, ISSN 1389-9600, 10/2018, Volume 17, Issue 4, pp. 567 - 567
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s10689-018-0074-6 
ONCOLOGY | GENETICS & HEREDITY | Heterozygote | Mutation | Colorectal Neoplasms, Hereditary Nonpolyposis | Mismatch Repair Endonuclease PMS2 - genetics | Humans | Liver | Index Medicus
Journal Article
International Journal of Cancer, ISSN 0020-7136, 08/2011, Volume 129, Issue 3, pp. 659 - 670
Journal Article
Journal Article
Familial Cancer, ISSN 1389-9600, 10/2016, Volume 15, Issue 4, pp. 587 - 591
Journal Article
Human mutation, ISSN 1059-7794, 2016, Volume 37, Issue 11, pp. 1162 - 1179
Journal Article
Journal Article
Journal Article
Molecular Carcinogenesis, ISSN 0899-1987, 12/2017, Volume 56, Issue 12, pp. 2663 - 2668
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 10/2008, Volume 205, Issue 11, pp. 2465 - 2472
Immunoglobulin (Ig) class switch recombination (CSR) deficiencies are rare primary immunodeficiencies characterized by the lack of switched isotype... 
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN MISMATCH REPAIR | SOMATIC HYPERMUTATION | MECHANISM | MICE DEFICIENT | MUTATIONS