Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum. - Wikidata - awgldk - TriplyDB

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

http://www.wikidata.org/entity/Q37326213

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Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing.Targeted DNA Sequencing Detects Mutations Related to Susceptibility among Familial Non-medullary Thyroid Cancer Study of apoptosis-related interactions in colorectal cancer.Thyroid cancer in a patient with Lynch syndrome - case report and literature review.Hepatocellular carcinoma as extracolonic manifestation of Lynch syndrome indicates SEC63 as potential target gene in hepatocarcinogenesis.Tumor development in Japanese patients with Lynch syndrome.Molecular Profiling of Synchronous Colon Cancers and Anaplastic Thyroid Cancer in a Patient with Lynch Syndrome.Mismatch repair single nucleotide polymorphisms and thyroid cancer susceptibility.

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Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum.

http://www.wikidata.org/entity/Q37326213

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 15 February 2008

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Thyroid cancer in a patient wi ...... ome expanding tumour spectrum.

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Thyroid cancer in a patient wi ...... ome expanding tumour spectrum.

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Thyroid cancer in a patient wi ...... ome expanding tumour spectrum.

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Thyroid cancer in a patient wi ...... ome expanding tumour spectrum.

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Hereditary Cancer in Clinical Practice

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Thyroid cancer in a patient wi ...... ome expanding tumour spectrum.

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Arend Karrenbeld

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Bart Mol

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Johanna C Herkert

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Rein P Stulp

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Rolf H Sijmons

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Yvonne J Vos

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P2860

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

Microsatellite instability in a pleomorphic rhabdomyosarcoma in a patient with hereditary non-polyposis colorectal cancer.

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.

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

Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.

A case of Muir-Torre syndrome associated with mucinous hepatic cholangiocarcinoma and a novel germline mutation of the MSH2 gene.

Cancer risk in mutation carriers of DNA-mismatch-repair genes.

The molecular basis of Turcot's syndrome.

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.

Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis.

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