Researchclopedia
Research
Researchers
Institutions
Topics
Submit
About
Search...
⌘
K
Command Palette
Search for a command to run...
Back to research
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
2011
528 citations
Journal Article
green Open Access
Field-Weighted Citation Impact:
34.25
Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma | Researchclopedia
·
Hospital de León
Rocío Ramos‐Medina
·
Spanish National Cancer Research Centre
Daniela Caronia
·
Spanish National Cancer Research Centre
Guillermo Pita
·
Spanish National Cancer Research Centre
Álvaro Gómez-Graña
·
Spanish National Cancer Research Centre
Aguirre A. de Cubas
·
Spanish National Cancer Research Centre
Lucía Inglada‐Pérez
·
Centre for Biomedical Network Research on Rare Diseases
Agnieszka Maliszewska
·
Spanish National Cancer Research Centre
Elisa Taschin
·
Istituto Oncologico Veneto
Sara Bobisse
·
Cancer Clinic
Giuseppe Pica
·
University of Foggia
Paola Loli
·
Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
Rafael Hernández-Lavado
·
Hospital Universitario Infanta Cristina
José Ángel Díaz
·
Hospital Clínico San Carlos
Mercedes Gómez‐Morales
·
Universidad de Granada
Anna González‐Neira
·
Spanish National Cancer Research Centre
Giovanna Roncador
·
Spanish National Cancer Research Centre
Cristina Rodríguez‐Antona
·
Spanish National Cancer Research Centre
Javier Benı́tez
·
Spanish National Cancer Research Centre
Massimo Mannelli
·
Tumour Institute of Tuscany
Giuseppe Opocher
·
University of Padua
Mercedes Robledo
·
Centre for Biomedical Network Research on Rare Diseases
Alberto Cascón
·
Spanish National Cancer Research Centre