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Article

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma families

5 Apr 2004

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15064708
DOI: 10.1038/sj.onc.1207591

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Somatic loss of maternal chromosome 11 causes parent-of-origin-dependent inheritance in SDHD-linked paraganglioma and phaeochromocytoma familiesPMID 15064708Read ↗

Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytomaSemantic proximity Read ↗

Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas.Semantic proximity Read ↗

A Novel Targeted Sequence for Chromosome 11p15.5 Maternal Loss in SDHD-Related Paragangliomas.Semantic proximity Read ↗

Disomy as the genetic underlying mechanisms of loss of heterozigosity in SDHD-paragangliomas.Semantic proximity Read ↗

Molecular analysis of pheochromocytoma after maternal transmission of SDHD mutation elucidates mechanism of parent-of-origin effect.Semantic proximity Read ↗

Paraganglioma and pheochromocytoma upon maternal transmission of SDHDmutationsSemantic proximity Read ↗

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene.Semantic proximity Read ↗

Germline SDHD mutation in familial phaeochromocytomaSemantic proximity Read ↗

Distortion in transmission of pathogenic SDHB- and SDHD-mutated alleles from parent to offspring.Semantic proximity Read ↗

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.Semantic proximity Read ↗

Fine mapping of a putatively imprinted gene for familial non-chromaffin paragangliomas to chromosome 11q13.1: evidence for genetic heterogeneitySemantic proximity Read ↗

Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.Semantic proximity Read ↗

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