Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma-Reference-Cited by-同舟云学术

Incomplete penetrance of a novel SDHD variation causing familial head and neck paraganglioma

Published:2021-05-05 Issue:5 Volume:46 Page:1044-1049
ISSN:1749-4478
Container-title:Clinical Otolaryngology
language:en
Short-container-title:Clin Otolaryngol

Author:

Koenighofer Martin¹^ORCID,Parzefall Thomas¹^ORCID,Frohne Alexandra²^ORCID,Frei Elisabeth²^ORCID,Schoefer Christian²^ORCID,Laccone Franco³^ORCID,Feil Patricia⁴^ORCID,Frei Klemens¹^ORCID,Lucas Trevor²^ORCID

Affiliation:

1. Department of Otorhinolaryngology, Head and Neck Surgery Medical University of Vienna Vienna Austria

2. Center of Anatomy and Cell biology Medical University of Vienna Vienna Austria

3. Department of Medical Genetics Medical University of Vienna Vienna Austria

4. Department of Pediatric Surgery Medical University of Vienna Vienna Austria

Publisher

Wiley

Subject

Otorhinolaryngology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/coa.13782

Reference28 articles.

1. A Decade (2001-2010) of Genetic Testing for Pheochromocytoma and Paraganglioma

2. Paragangliomas of the head and neck

3. Benign Paragangliomas: Clinical Presentation and Treatment Outcomes in 236 Patients

4. An overview of 20 years of genetic studies in pheochromocytoma and paraganglioma

5. PheoSeq

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