Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.

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Haplotype analysis suggest that the MLH1 c.2059C > T mutation is a Swedish founder mutation.

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Haplotype analysis suggest tha ...... is a Swedish founder mutation.

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Haplotype analysis suggest tha ...... is a Swedish founder mutation.

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Haplotype analysis suggest tha ...... is a Swedish founder mutation.

@en

Haplotype analysis suggest tha ...... is a Swedish founder mutation.

@nl

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Haplotype analysis suggest tha ...... is a Swedish founder mutation.

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Haplotype analysis suggest tha ...... is a Swedish founder mutation.

@nl

P1476

Haplotype analysis suggest tha ...... is a Swedish founder mutation

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Annika Lindblom

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Elke Holinski-Feder

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Ian R Berry

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Jenny von Salomé

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Markku Keihäs

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Moni Morak

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Stéphanie Baert-Desurmont

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Tao Liu

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P2860

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

Analysis of protein-coding genetic variation in 60,706 humans

Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes.

The founder mutation MSH2*1906G-->C is an important cause of hereditary nonpolyposis colorectal cancer in the Ashkenazi Jewish population.

Founding mutations and Alu-mediated recombination in hereditary colon cancer.

Lynch syndrome: an updated review

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome.

Recurrent germline mutation in MSH2 arises frequently de novo.

Founder mutations among the Dutch.

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s10689-017-0067-x

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531-537

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scholarly article

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10.1007/S10689-017-0067-X

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P433

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P478

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Jukka S Moilanen

Kristina Lagerstedt Robinson

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2018-10-01T00:00:00Z

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29288294

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6182575

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