Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium. [electronic resource]
Producer: 20160627Description: 275-84 p. digitalISSN:- 1572-0241
- Adaptor Proteins, Signal Transducing -- genetics
- Adenocarcinoma -- etiology
- Adenoma -- etiology
- Adenosine Triphosphatases -- genetics
- Adolescent
- Adult
- Alleles
- Brain Neoplasms -- complications
- Child
- Child, Preschool
- Colorectal Neoplasms -- complications
- DNA Repair Enzymes -- genetics
- DNA-Binding Proteins -- genetics
- Female
- Germ-Line Mutation
- Glioma -- etiology
- Humans
- Intestinal Neoplasms -- etiology
- Intestine, Small -- surgery
- Kidney Neoplasms -- etiology
- Leukemia -- etiology
- Lymphoma -- etiology
- Male
- Melanoma -- etiology
- Mismatch Repair Endonuclease PMS2
- MutL Protein Homolog 1
- Neoplastic Syndromes, Hereditary -- complications
- Nuclear Proteins -- genetics
- Phenotype
- Prospective Studies
- Retrospective Studies
- Wilms Tumor -- etiology
- Young Adult
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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