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Aufsätze
1
Causes of death of mutation carriers in Finnish Lynch syndrome families
von: Pylvänäinen, Kirsi
2012, in:
Familial cancer
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2
Psychosocial consequences of predictive genetic testing for lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study
von: Aktan-Collan, Katja
2013, in:
Familial cancer
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3
Sharing genetic risk with next generation: mutation-positive parents’ communication with their offspring in Lynch Syndrome
von: Aktan-Collan, Katja I.
2010, in:
Familial cancer
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4
Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial
von: Burn, John
2020, in:
Effects of shape functions on flexural–torsional buckling of fixed circular arches
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5
Colorectal cancer incidence in path_MLH1 carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database report
von: Seppälä, Toni
2017, in:
Hereditary cancer in clinical practice
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6
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database report
von: Dominguez-Valentin, Mev
2019, in:
Hereditary cancer in clinical practice
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7
No Difference in Colorectal Cancer Incidence or Stage at Detection by Colonoscopy Among 3 Countries With Different Lynch Syndrome Surveillance Policies
von: Engel, Christoph
2018, in:
Ubiquitin protease Ubp8 is necessary for
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8
Associations of Pathogenic Variants in MLH1, MSH2, and MSH6 With Risk of Colorectal Adenomas and Tumors and With Somatic Mutations in Patients With Lynch Syndrome
von: Engel, Christoph
2020, in:
Ubiquitin protease Ubp8 is necessary for
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9
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report
von: Seppälä, Toni T.
2019, in:
Hereditary cancer in clinical practice
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10
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report
von: Seppälä, Toni T.
17 March 2021, in:
European journal of cancer
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11
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report
von: Seppälä, Toni T.
2021, in:
European journal of cancer
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12
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report
von: Dominguez-Valentin, Mev
April 2021, in:
Genetics in medicine
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13
Colorectal cancer incidences in Lynch syndrome: a comparison of results from the prospective lynch syndrome database and the international mismatch repair consortium
von: Møller, Pål
2022, in:
Hereditary cancer in clinical practice
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14
Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study
von: Win, Aung Ko
2021, in:
My
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