(Q35439138)

8 August 2017

Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas (English)

1 reference

8 August 2017

B E Baysal

1

1 reference

8 August 2017

J E Willett-Brozick

2

1 reference

8 August 2017

E C Lawrence

3

1 reference

8 August 2017

C M Drovdlic

4

1 reference

8 August 2017

S A Savul

5

1 reference

8 August 2017

D R McLeod

6

1 reference

8 August 2017

H A Yee

7

1 reference

8 August 2017

D E Brackmann

8

1 reference

8 August 2017

W H Slattery

9

1 reference

8 August 2017

E N Myers

10

1 reference

8 August 2017

R E Ferrell

11

1 reference

8 August 2017

W S Rubinstein

12

1 reference

8 August 2017

language of work or name

English

0 references

publication date

1 March 2002

1 reference

Journal of Medical Genetics

8 August 2017

1 reference

8 August 2017

39

1 reference

8 August 2017

3

1 reference

8 August 2017

178-183

1 reference

Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma

8 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

A high-resolution integrated map spanning the SDHD gene at 11q23: a 1.1-Mb BAC contig, a partial transcript map and 15 new repeat polymorphisms in a tumour-suppressor region

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Genetic analysis in the diagnosis of familial paragangliomas

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Familial carotid body tumors: case report and epidemiologic review

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Hyperplasia of vagal and carotid body paraganglia in patients with chronic hypoxemia

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Novel mutations in the SDHD gene in pedigrees with familial carotid body paraganglioma and sensorineural hearing loss

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Novel mutations and the emergence of a common mutation in the SDHD gene causing familial paraganglioma

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

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

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1735061

Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma

26 September 2018

1 reference

12 December 2020

Proportion of heritable paraganglioma cases and associated clinical characteristics

1 reference

12 December 2020

Chief cell hyperplasia in the human carotid body at high altitudes; physiologic and pathologic significance

1 reference

12 December 2020

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

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

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

Familial paragangliomas: linkage to chromosome 11q23 and clinical implications

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.39.3.178

1 reference

8 August 2017

1 reference

8 August 2017

1 reference