(Q44830441)

English

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

scientific article published in May 2004

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scholarly article

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26 December 2019

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

1 reference

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26 December 2019

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Ekaterina S. Jordanova

2

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26 December 2019

Ekaterina S. Jordanova

3

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26 December 2019

Pancras C.W. Hogendoorn

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26 December 2019

Peter E Taschner

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26 December 2019

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Erik F Hensen

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26 December 2019

Ivonne J H M van Minderhout

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26 December 2019

Andel G L van der Mey

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26 December 2019

Cees J Cornelisse

9

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26 December 2019

Peter Devilee

8

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26 December 2019

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1 May 2004

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26 December 2019

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26 December 2019

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26 December 2019

23

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26 December 2019

4076-4083

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26 December 2019

https://scigraph.springernature.com/pub.10.1038/sj.onc.1207591

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Comparative genomic hybridization reveals frequent losses of chromosomes 1p and 3q in pheochromocytomas and abdominal paragangliomas, suggesting a common genetic etiology

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Founder effect at PGL1 in hereditary head and neck paraganglioma families from the Netherlands

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Organization and evolution of alpha satellite DNA from human chromosome 11.

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Paragangliomas of the head and neck region show complete loss of heterozygosity at 11 q22-q23 in chief cells and the flow-sorted dna aneuploid fraction

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Allelic phasing of a mouse chromosome 11 deficiency influences p53 tumorigenicity

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Allelotype of head and neck paragangliomas: Allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locusPGL

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Hemizygous deletions in the HLA region account for loss of heterozygosity in the majority of diffuse large B-cell lymphomas of the testis and the central nervous system

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Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome

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Identifiers

10.1038/SJ.ONC.1207591

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