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Article

Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation

1 Feb 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 14762794
DOI: 10.1053/j.gastro.2003.11.008

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Related research

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Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutationPMID 14762794Read ↗

Germline epimutation of MLH1 in individuals with multiple cancersSemantic proximity Read ↗

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

Homozygosity at variant MLH1 can lead to secondary mutation in NF1, neurofibromatosis type I and early onset leukemiaSemantic proximity Read ↗

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Pediatric Lynch syndrome: Clinical, genotypic, and left-sided patterns of colorectal cancer.Semantic proximity Read ↗

MSH2, MSH6, MLH1, and PMS2 immunohistochemistry as highly sensitive screening method for DNA mismatch repair deficiency syndromes in pediatric high-grade gliomaSemantic proximity Read ↗

Germline MUTYH mutations and high‐grade gliomas: Novel evidence for a potential associationSemantic proximity Read ↗

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1.Semantic proximity Read ↗

Prophylactic total gastrectomy for individuals with germline CDH1 mutationSemantic proximity Read ↗

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeSemantic proximity Read ↗

BRAF-V600E is not involved in the colorectal tumorigenesis of HNPCC in patients with functional MLH1 and MSH2 genesSemantic proximity Read ↗

Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. Online.Semantic proximity Read ↗

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