Associated Papers
New Insights into the Clinical Characterization of SDHAF2-related Familial Paraganglioma Syndrome.
Fernandez-Pombo A et al.
The Journal of Clinical Endocrinology and Metabolism, 2025
Tumor detection rates in screening of individuals with SDHx-related hereditary paraganglioma-pheochromocytoma syndrome.
Greenberg SE et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2020
32741965 (PubMed )
Supplement: NIHMS1619684-supplement-Supplemental_Tables_S1-S3.xlsx › Table_S3
A Family With a Carotid Body Paraganglioma and Thyroid Neoplasias With a New SDHAF2 Germline Variant.
Wolf KI et al.
Journal of the Endocrine Society, 2019
Head and Neck Paragangliomas: Patterns of Otolaryngology Referrals for Genetic Testing Over 2 Decades.
Smith JD et al.
Oto Open, 0
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