(Q51776685)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

Germline mutations and genotype-phenotype correlations in patients with apparently sporadic pheochromocytoma/paraganglioma in Korea (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Sung Wook Park

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Moon-Woo Seong

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Jae Hyun Bae

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

author name string

J H Kim

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

K E Lee

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

H J Choi

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

S H Choi

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

S W Kim

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Cs Shin

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

S Y Kim

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

publication date

15 November 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

volume

86

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

page(s)

482-486

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

Evaluation of SDHB, SDHD and VHL gene susceptibility testing in the assessment of individuals with non-syndromic phaeochromocytoma, paraganglioma and head and neck paraganglioma

28 February 2020

cites work

1 reference

Germ-line mutations in nonsyndromic pheochromocytoma

21 January 2018

1 reference

Genetic testing in pheochromocytoma or functional paraganglioma

21 January 2018

1 reference

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

21 January 2018

1 reference

Prevalence of germline mutations in patients with pheochromocytoma or abdominal paraganglioma and sporadic presentation: a population-based study in Western Sweden

21 January 2018

1 reference

Genetic analyses of apparently sporadic pheochromocytomas: the Rotterdam experience

21 January 2018

1 reference

Clinically guided genetic screening in a large cohort of italian patients with pheochromocytomas and/or functional or nonfunctional paragangliomas

21 January 2018

1 reference

A decade (2001-2010) of genetic testing for pheochromocytoma and paraganglioma

21 January 2018

1 reference

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

21 January 2018

1 reference

Clinical review 155: Pheochromocytoma in Von Hippel-Lindau disease

21 January 2018

1 reference

Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2

21 January 2018

1 reference

An update on the genetics of pheochromocytoma

21 January 2018

1 reference

The genetics of phaeochromocytoma: using clinical features to guide genetic testing.

21 January 2018

1 reference

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/CGE.12304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24134185%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

1 reference