SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma (Q34092600)

31 July 2017

SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma (English)

1 reference

31 July 2017

1 reference

24

1 reference

31 July 2017

21

Peter Devilee

0 references

Alberto Cascón

object named as

Alberto Cascon

3

0 references

Peter de Knijff

object named as

Peter de Knijff

18

0 references

Jacques W M Lenders

19

object named as

Jacques W M Lenders

1 reference

31 July 2017

9

Lies H Hoefsloot

1 reference

31 July 2017

20

Cor W R J Cremers

1 reference

31 July 2017

2

Henricus P M Kunst

1 reference

31 July 2017

8

Henri J L M Timmers

1 reference

31 July 2017

1

Jean-Pierre Bayley

1 reference

31 July 2017

23

Ronald R de Krijger

1 reference

31 July 2017

22

Winand N M Dinjens

1 reference

31 July 2017

6

Esther Korpershoek

1 reference

31 July 2017

5

José Gaal

1 reference

31 July 2017

Maria Lourdes Sampietro

4

1 reference

31 July 2017

Adolfo Hinojar-Gutierrez

7

1 reference

31 July 2017

Mario A Hermsen

10

1 reference

31 July 2017

Carlos Suárez

11

1 reference

31 July 2017

A Karim Hussain

12

1 reference

31 July 2017

Annette H J T Vriends

13

1 reference

31 July 2017

Frederik J Hes

14

1 reference

31 July 2017

Jeroen C Jansen

15

1 reference

31 July 2017

Carli M Tops

16

1 reference

31 July 2017

Eleonora P Corssmit

17

1 reference

31 July 2017

11 January 2010

1 reference

Lancet Oncology Commission

31 July 2017

1 reference

31 July 2017

11

1 reference

31 July 2017

366-372

1 reference

31 July 2017

4

1 reference

The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.

31 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

IDH1 and IDH2 mutations in gliomas

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Gross SDHB deletions in patients with paraganglioma detected by multiplex PCR: a possible hot spot?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

The first Dutch SDHB founder deletion in paraganglioma-pheochromocytoma patients

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Somatic SDHB mutation in an extraadrenal pheochromocytoma

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

SIFT: Predicting amino acid changes that affect protein function

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Prediction of deleterious human alleles

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Worldwide human relationships inferred from genome-wide patterns of variation

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Genetic screening for pheochromocytoma: should SDHC gene analysis be included?

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2810%2970007-3

7 January 2021

10.1016/S1470-2045(10)70007-3

Identifiers

DOI

1 reference

release_637abzcb2ngifcmmh5ewzuvqh4

31 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/637abzcb2ngifcmmh5ewzuvqh4

24 November 2022

mapped directly with Wikidata item

1 reference