Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene (Q43629703)

25 November 2017

title

Nearly all hereditary paragangliomas in the Netherlands are caused by two founder mutations in the SDHD gene (English)

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25 November 2017

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Devilee P

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25 November 2017

Taschner PE

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25 November 2017

Jansen JC

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25 November 2017

Baysal BE

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25 November 2017

Bosch A

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25 November 2017

Rosenberg EH

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25 November 2017

Bröcker-Vriends AH

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25 November 2017

van Der Mey AG

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25 November 2017

van Ommen GJ

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25 November 2017

Cornelisse CJ

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25 November 2017

publication date

1 July 2001

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Genes, Chromosomes and Cancer

25 November 2017

published in

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25 November 2017

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25 November 2017

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25 November 2017

page(s)

274-281

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Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

25 November 2017

cites work

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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

21 January 2018

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Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

21 January 2018

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

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The distribution of charged amino acids in mitochondrial inner-membrane proteins suggests different modes of membrane integration for nuclearly and mitochondrially encoded proteins

21 January 2018

1 reference

Familial carotid body tumors: case report and epidemiologic review

21 January 2018

1 reference

A gene subject to genomic imprinting and responsible for hereditary paragangliomas maps to chromosome 11q23-qter

21 January 2018

1 reference

Paragangliomas of the head and neck region. A pathologic study of tumors from 71 patients

21 January 2018

1 reference

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

21 January 2018

1 reference

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

Imprinting in Prader-Willi and Angelman syndromes

21 January 2018

1 reference

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

21 January 2018

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First experiences with genetic counselling based on predictive DNA diagnosis in hereditary glomus tumours (paragangliomas)

21 January 2018

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Amounts of mitochondrial DNA and abundance of some mitochondrial gene transcripts in early mouse embryos

21 January 2018

1 reference

Human mitochondrial complex I in health and disease

21 January 2018

1 reference

Genomic imprinting in hereditary glomus tumours: evidence for new genetic theory

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Analysis of a second family with hereditary non-chromaffin paragangliomas locates the underlying gene at the proximal region of chromosome 11q

21 January 2018

1 reference

PGL3, a third, not maternally imprinted locus in autosomal dominant paraganglioma

21 January 2018

1 reference

Further localization of the gene for hereditary paragangliomas and evidence for linkage in unrelated families

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GCC.1144

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25 November 2017

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