Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

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Same MSH2 Gene Mutation But Variable Phenotypes in 2 Families With Lynch Syndrome: Two Case Reports and Review of Genotype-Phenotype Correlation.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

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Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

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Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

@en

Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

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Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

@en

Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

@nl

P1476

Same MSH2 Gene Mutation But Va ...... enotype-Phenotype Correlation.

@en

P2093

Francesca Duraturo

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Marina De Rosa

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Raffaella Liccardo

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P2860

The biological complexity of colorectal cancer: insights into biomarkers for early detection and personalized care

Incomplete Segregation of MSH6 Frameshift Variants with Phenotype of Lynch Syndrome.

The genetic basis of Lynch syndrome and its implications for clinical practice and risk management.

A review on the molecular diagnostics of Lynch syndrome: a central role for the pathology laboratory.

Genetics, diagnosis and management of colorectal cancer (Review).

Microsatellite instability and DNA mismatch repair deficiency testing in hereditary and sporadic gastrointestinal cancers.

Novel Implications in Molecular Diagnosis of Lynch Syndrome.

The association of low penetrance genetic risk modifiers with colorectal cancer in lynch syndrome patients: a systematic review and meta-analysis.

The role of mutation analysis of the APC gene in the management of FAP patients. A controversial issue.

Contribution of large genomic rearrangements in Italian Lynch syndrome patients: characterization of a novel alu-mediated deletion.

P304

1179547617753943

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scholarly article

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10.1177/1179547617753943

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P478

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P577

2018-01-23T00:00:00Z

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29383008

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5784535

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