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Predictive functional assay-based classification of PMS2 variants in Lynch syndrome.
Rayner, Emily; Tiersma, Yvonne; Fortuno, Cristina; van Hees-Stuivenberg, Sandrine; Drost, Mark; Thompson, Bryony; Spurdle, Amanda B; de Wind, Niels.
Affiliation
  • Rayner E; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Tiersma Y; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Fortuno C; Princess Maxima Center for Child Oncology, Utrecht, the Netherlands.
  • van Hees-Stuivenberg S; QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.
  • Drost M; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Thompson B; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands.
  • Spurdle AB; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands.
  • de Wind N; Department of Pathology, Royal Melbourne Hospital, Parkville, Victoria, Australia.
Hum Mutat ; 43(9): 1249-1258, 2022 09.
Article in En | MEDLINE | ID: mdl-35451539
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms, Hereditary Nonpolyposis / Mismatch Repair Endonuclease PMS2 Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Type: Article Affiliation country: Netherlands
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms, Hereditary Nonpolyposis / Mismatch Repair Endonuclease PMS2 Type of study: Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2022 Type: Article Affiliation country: Netherlands