Tumor Detection Rates in Screening of Individuals with SDHx-related Hereditary Paraganglioma-Pheochromocytoma Syndrome

PURPOSE: Minimal data exist regarding the efficacy of screening protocols for individuals with SDHx germline pathogenic variants with Hereditary Paraganglioma-Pheochromocytoma Syndrome. This study aimed to evaluate the SDHx-related tumor detection rate in individuals undergoing clinical screening pr...

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發表在:Genet Med
Main Authors: Greenberg, Samantha E., Jacobs, Michelle F., Wachtel, Heather, Anson, Amanda, Buchmann, Luke, Cohen, Debbie L., Bonanni, Maria, Bennett, Bonita, Naumer, Anne, Schaefer, Amanda M., Kohlmann, Wendy, Nathanson, Katherine L., Else, Tobias, Fishbein, Lauren
格式: Artigo
語言:Inglês
出版: 2020
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC7710583/
https://ncbi.nlm.nih.gov/pubmed/32741965
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-020-0921-3
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