(Q43050008)

13 November 2017

Are we overestimating the penetrance of mutations in SDHB? (English)

1 reference

13 November 2017

6

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13 November 2017

7

1 reference

13 November 2017

2

Roger L Milne

1 reference

13 November 2017

Francesca Schiavi

1

0 references

Alberto Cascón

object named as

Alberto Cascón

8

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Maurizio Castellano

object named as

Maurizio Castellano

5

0 references

author name string

Emma Anda

3

1 reference

PubMed ID

20513144

13 November 2017

Pilar Blay

4

1 reference

PubMed ID

20513144

13 November 2017

language of work or name

1 reference

1 June 2010

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13 November 2017

1 reference

13 November 2017

31

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13 November 2017

761-762

1 reference

13 November 2017

6

1 reference

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

13 November 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Genetics of pheochromocytoma and paraganglioma in Spanish patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Programs for pedigree analysis: Mendel, Fisher, and dGene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Germline SDHB mutations and familial renal cell carcinoma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHD.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Penetrance and clinical consequences of a gross SDHB deletion in a large family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.21269

7 January 2021

Identifiers

DOI

10.1002/HUMU.21269

1 reference

13 November 2017

1 reference

PubMed ID

20513144