A Decade (2001-2010) of Genetic Testing for Pheochromocytoma and Paraganglioma
Alexandre Buffet(Inserm), Anne‐Paule Gimenez‐Roqueplo(Délégation Paris 5), Magali Boussion(Assistance Publique – Hôpitaux de Paris), Judith Favier(Inserm), Nasséra Abermil(Centre National de la Recherche Scientifique), Valérie Boccio(Assistance Publique – Hôpitaux de Paris), Valérie Nau, Xavier Jeunemaı̂tre(Délégation Paris 5), Nelly Burnichon(Inserm), Christophe Simian(Assistance Publique – Hôpitaux de Paris), C. Travers(Inserm), Nelly Le Pottier(Assistance Publique – Hôpitaux de Paris), Annabelle Vénisse(Assistance Publique – Hôpitaux de Paris), I. Roncellin(Assistance Publique – Hôpitaux de Paris)
Cited by 121
Related Papers
The 2017 international classification of the Ehlers–Danlos syndromes
|American Journal of Medical Genetics Part C Seminars in Medical Genetics|2017|1.9k
The ratio of the nucleon structure functions F2N for iron and deuterium
|Physics Letters B|1983|1.1k
Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma
|Cancer Cell|2017|791
SDH Mutations Establish a Hypermethylator Phenotype in Paraganglioma
|Cancer Cell|2013|772