The mutational spectrum of Lynch syndrome in cyprus. - Wikidata - awgldk - TriplyDB

The mutational spectrum of Lynch syndrome in cyprus.

The mutational spectrum of Lynch syndrome in cyprus.

http://www.wikidata.org/entity/Q34062115

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The mutational spectrum of Lynch syndrome in cyprus.

http://www.wikidata.org/entity/Q34062115

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2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

The mutational spectrum of Lynch syndrome in cyprus.

@ast

The mutational spectrum of Lynch syndrome in cyprus.

@en

The mutational spectrum of Lynch syndrome in cyprus.

@nl

type

label

The mutational spectrum of Lynch syndrome in cyprus.

@ast

The mutational spectrum of Lynch syndrome in cyprus.

@en

The mutational spectrum of Lynch syndrome in cyprus.

@nl

prefLabel

The mutational spectrum of Lynch syndrome in cyprus.

@ast

The mutational spectrum of Lynch syndrome in cyprus.

@en

The mutational spectrum of Lynch syndrome in cyprus.

@nl

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The mutational spectrum of Lynch syndrome in cyprus.

@en

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Andreas Hadjisavvas

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Chrystalla Philippou

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Demetris Papamichael

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Elena Spanou

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Eleni Kakouri

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Georgios Ioannidis

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Ioanna Neophytou

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Kyriacos Kyriacou

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

Maria A Loizidou

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Panteleimon Kountourakis

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P2860

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome

Hereditary and familial colon cancer

Cancer incidence and mortality patterns in Europe: estimates for 40 countries in 2012

Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and characterization of an American founder genomic deletion of the MSH2 gene.

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

Report from the Jerusalem workshop on Lynch syndrome-hereditary nonpolyposis colorectal cancer.

The molecular basis of Turcot's syndrome.

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

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