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10.4149/neo_2017_215 OR Absence of BRAF mutation in pheochromocytoma and paraganglioma Dotaz Zobrazit nápovědu

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Článek

Absence of BRAF mutation in pheochromocytoma and paraganglioma

Vosecká, Tatiana
Autor Vosecká, Tatiana Department of Pediatric Hematology and Oncology, 2nd Medical School, Charles University and University Hospital Motol, Prague
Vícha, Aleš, 1971-
Autor Autorita ORCID Department of Pediatric Hematology and Oncology, 2nd Medical School, Charles University and University Hospital Motol, Prague
Zelinka, Tomáš
Autor Autorita ORCID 3rd Department of Medicine - Department of Endocrinology and Metabolism, First Faculty of Medicine, Charles University in Prague and General Universisty of Hospital in Prague
Jencova, P
Autor Jencova, P Department of Pediatric Hematology and Oncology, 2nd Medical School, Charles University and University Hospital Motol, Prague
Pacák, Karel, 1958-
Autor Autorita ORCID Section on Medical Neuroendocrinology, Eunice Kennedy Shriver Narional Institute of Child Health & Human Development (NICHD), National Institutes of Health, Bethesda, Maryland, USA
Dušková, Jaroslava, 1952-
Autor Autorita ORCID Institute of Pathology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
Beneš, Jiří, 1982-
Autor Autorita ORCID Department of Radiology, 1st Faculty of Medicine, Charles University in Prague and General University in prague Institute of Anatomy, 1st Faculty of Medicine, Charles University in Prague
Guha, A
Autor Guha, A Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
Staněk, Libor
Autor Autorita Department of Oncology, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague
Kohoutová, Milada, 1948-
Autor Autorita ORCID Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague

Neoplasma. 2017 ; 64 (2) : 278-282.

ISSN 0028-2685
Medvik
Zdroj

MeSH
feochromocytom * diagnóza genetika MeSH
klinická studie jako téma MeSH
lidé MeSH
mutace MeSH
paragangliom * diagnóza genetika MeSH
polymerázová řetězová reakce MeSH
protoonkogenní proteiny B-raf genetika MeSH
sekvenční analýza DNA MeSH
Check Tag
lidé MeSH
Publikační typ
práce podpořená grantem MeSH

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10.4149/neo_2017_215 OR Absence of BRAF mutation in pheochromocytoma and paraganglioma Dotaz Zobrazit nápovědu

Přesná shoda Sémantické

10.4149/neo_2017_215 OR Absence of BRAF mutation in pheochromocytoma and paraganglioma Dotaz Zobrazit nápovědu Přesná shoda Sémantické

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10.4149/neo_2017_215 OR Absence of BRAF mutation in pheochromocytoma and paraganglioma Dotaz Zobrazit nápovědu

Přesná shoda Sémantické