Correspondence on "Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database" by Dominguez-Valentin et al.

Chambuso, Ramadhani; Kaambo, Evelyn; Rebello, George; Ramesar, Raj

Correspondence on "Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database" by Dominguez-Valentin et al.

Chambuso, Ramadhani; Kaambo, Evelyn; Rebello, George; Ramesar, Raj.

Afiliación

Chambuso R; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa; MRC Unit for Genomic and Precision Medicine, Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa. Electronic address
Kaambo E; Department of Biochemistry and Medical Microbiology, School of Medicine, University of Namibia, Windhoek, Namibia; Division of Medical Virology, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Rebello G; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa; MRC Unit for Genomic and Precision Medicine, Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Ramesar R; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa; MRC Unit for Genomic and Precision Medicine, Division of Human Genetics, Department of Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa; Division of Human

Genet Med ; 24(5): 1148-1150, 2022 05.

Article en En | MEDLINE | ID: mdl-35168886

Asunto(s)

Neoplasias Colorrectales Hereditarias sin Poliposis; Neoplasias Colorrectales Hereditarias sin Poliposis/genética; Neoplasias Colorrectales Hereditarias sin Poliposis/patología; Reparación de la Incompatibilidad de ADN/genética; Heterocigoto; Humanos; Endonucleasa PMS2 de Reparación del Emparejamiento Incorrecto/genética; Homólogo 1 de la Proteína MutL/genética; Proteína 2 Homóloga a MutS/genética; Estudios Prospectivos

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Med Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article

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