(Q34386460)

1 August 2017

title

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

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head and neck paraganglioma

1 August 2017

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8

Devilee P

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1 August 2017

van Schothorst EM

1

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1 August 2017

Jansen JC

2

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1 August 2017

Grooters E

3

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1 August 2017

Prins DE

4

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1 August 2017

Wiersinga JJ

5

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1 August 2017

van der Mey AG

6

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1 August 2017

van Ommen GJ

7

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1 August 2017

Cornelisse CJ

9

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1 August 2017

language of work or name

English

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publication date

1 August 1998

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American Journal of Human Genetics

1 August 2017

published in

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1 August 2017

volume

63

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1 August 2017

issue

2

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1 August 2017

page(s)

468-473

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A high-resolution STS, EST, and gene-based physical map of the hereditary paraganglioma region on chromosome 11q23.

1 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

A high proportion of novel mutations in BRCA1 with strong founder effects among Dutch and Belgian hereditary breast and ovarian cancer families

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Familial paragangliomas of the head and neck

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Familial carotid body tumors: case report and epidemiologic review

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Carotid body tumors in humans: genetics and epidemiology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

MRI screening of kindred at risk of developing paragangliomas: support for genomic imprinting in hereditary glomus tumours

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Imprinted chromosomal regions of the human genome display sex-specific meiotic recombination frequencies.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Carrier detection of Batten disease (Juvenile neuronal ceroid-lipofuscinosis)

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377293

Rare disease genes--lessons and challenges

27 October 2018

1 reference

12 December 2020

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications

1 reference

12 December 2020

Concurrence of carotid body tumor and pheochromocytoma

1 reference

12 December 2020

Paragangliomas of the head and neck region: a clinical study of 69 patients

1 reference

12 December 2020

Multiple Simultaneous Paragangliomas of The Head and Neck in Association with Multiple Retroperitoneal Pheochromocytomas

1 reference

12 December 2020

Genetic aspects of nonchromaffin paraganglioma

1 reference

12 December 2020

Hypothyroidism and chemodectoma in father and daughter: a new syndrome of a coincidence?

1 reference

12 December 2020

Founder effect in a Belgian-Dutch fragile X population

1 reference

12 December 2020

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

1 reference

12 December 2020

Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region

1 reference

12 December 2020

The CEPH Consortium Linkage Map of Human Chromosome 11

1 reference

12 December 2020

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

12 December 2020

Identifiers

DOI

10.1086/301951

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1 August 2017

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1 August 2017

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