Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

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Phenotypic and genotypic heterogeneity of Lynch syndrome: a complex diagnostic challenge.Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome.

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Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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name

Screening for germline mutatio ...... by next generation sequencing.

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Screening for germline mutatio ...... by next generation sequencing.

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Screening for germline mutatio ...... by next generation sequencing.

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Screening for germline mutatio ...... by next generation sequencing.

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Screening for germline mutatio ...... by next generation sequencing.

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Screening for germline mutatio ...... by next generation sequencing.

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P1476

Screening for germline mutatio ...... by next generation sequencing.

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Ayslan Castro Brant

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Maria Isabel W Achatz

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Miguel Angelo Martins Moreira

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Naye Balzan Schneider

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Patrícia Ashton-Prolla

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Paulo Pimentel de Assumpção

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Renan Gomes

http://www.w3.org/2001/XMLSchema#string

Tatiane Pastor

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P2860

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

Evaluation of oligonucleotide sequence capture arrays and comparison of next-generation sequencing platforms for use in molecular diagnostics.

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.

Practical tools to implement massive parallel pyrosequencing of PCR products in next generation molecular diagnostics

Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.

Germline mutation analysis of MLH1 and MSH2 in Malaysian Lynch syndrome patients.

Clinical and Molecular Characterization of Brazilian Patients Suspected to Have Lynch Syndrome.

Whole Gene Capture Analysis of 15 CRC Susceptibility Genes in Suspected Lynch Syndrome Patients.

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s10689-017-0043-5

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387-394

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scholarly article

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10.1007/S10689-017-0043-5

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Ândrea Ribeiro-dos-santos

Bárbara Luisa Soares

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2017-09-20T00:00:00Z

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28932927

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Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

about

P2860

P2860

Screening for germline mutations in mismatch repair genes in patients with Lynch syndrome by next generation sequencing.

description

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type

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P1433

P1476

P2093

P2860

P2888

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P356

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P698

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P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698