(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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10

Devilee P

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25 November 2017

Taschner PE

1

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25 November 2017

Jansen JC

2

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25 November 2017

Baysal BE

3

1 reference

25 November 2017

Bosch A

4

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25 November 2017

Rosenberg EH

5

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25 November 2017

Bröcker-Vriends AH

6

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25 November 2017

van Der Mey AG

7

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25 November 2017

van Ommen GJ

8

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25 November 2017

Cornelisse CJ

9

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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

volume

31

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25 November 2017

issue

3

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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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

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

1 reference

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

1 reference

25 November 2017

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