(Q46782573)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16258955%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

title

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

1 reference

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8 January 2020

1 reference

Cristina Montero-Conde

2

1 reference

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Cristina Rodríguez-Antona

8 January 2020

6

1 reference

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8 January 2020

Beatriz Martinez-Delgado

7

1 reference

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8 January 2020

Mercedes Robledo

12

1 reference

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8 January 2020

Alberto Cascón

1

1 reference

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8 January 2020

Sergio Ruiz-Llorente

3

1 reference

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8 January 2020

author name string

Fátima Mercadillo

4

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8 January 2020

Rocío Letón

5

1 reference

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8 January 2020

Manuel Delgado

8

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8 January 2020

Alberto Díez

9

1 reference

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8 January 2020

Adela Rovira

10

1 reference

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8 January 2020

José Angel Díaz

11

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8 January 2020

publication date

1 March 2006

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Genes, Chromosomes and Cancer

8 January 2020

published in

1 reference

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8 January 2020

volume

45

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8 January 2020

issue

3

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8 January 2020

page(s)

213-219

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

8 January 2020

cites work

1 reference

7 January 2021

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

1 reference

7 January 2021

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

1 reference

7 January 2021

Molecular profiling of inflammatory breast cancer: identification of a poor-prognosis gene expression signature.

1 reference

7 January 2021

Clinical characteristics of pheochromocytoma patients with germline mutations in SDHD.

1 reference

7 January 2021

The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors

1 reference

7 January 2021

Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations

1 reference

7 January 2021

Large germline deletions of mitochondrial complex II subunits SDHB and SDHD in hereditary paraganglioma

1 reference

7 January 2021

Germ-line mutations in nonsyndromic pheochromocytoma

1 reference

7 January 2021

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

1 reference

7 January 2021

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

1 reference

7 January 2021

Multiple endocrine neoplasia: how many syndromes?

1 reference

7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

7 January 2021

Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma

1 reference

7 January 2021

Identifiers

DOI

10.1002/GCC.20283

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16258955%20AND%20SRC:MED&resulttype=core&format=json

8 January 2020

1 reference