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Article

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

23 Mar 2000

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 10763829
DOI: 10.1038/sj.onc.1203447

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 11 closest

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 genePMID 10763829Read ↗

A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts.Semantic proximity Read ↗

Drastic genetic instability of tumors and normal tissues in Turcot syndromeSemantic proximity Read ↗

Disruption of the APC gene by t(5;7) translocation in a Turcot familySemantic proximity Read ↗

Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.Semantic proximity Read ↗

Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2Semantic proximity Read ↗

PMS2 monoallelic mutation carriers: the known unknownSemantic proximity Read ↗

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.Semantic proximity Read ↗

Familial isolated hyperparathyroidism due to HRPT2 mutation.Semantic proximity Read ↗

Evidence for a recessive PMP22 point mutation in Charcot–Marie–Tooth disease type 1ASemantic proximity Read ↗

Turcot syndrome confirmed with molecular analysis.Semantic proximity Read ↗

Germline hMSH2 and differential somatic mutations in patients with Turcot's syndrome.Semantic proximity Read ↗

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