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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Neoplasms and SDHAF2[original query]
SDHAF2 mutations in familial and sporadic paraganglioma and phaeochromocytoma.
The Lancet. Oncology 2010 Apr 11 (4): 366-72.
Bayley Jean-Pierre, Kunst Henricus P M, Cascon Alberto, Sampietro Maria Lourdes, Gaal José, Korpershoek Esther, Hinojar-Gutierrez Adolfo, Timmers Henri J L M, Hoefsloot Lies H, Hermsen Mario A, Suárez Carlos, Hussain A Karim, Vriends Annette H J T, Hes Frederik J, Jansen Jeroen C, Tops Carli M, Corssmit Eleonora P, de Knijff Peter, Lenders Jacques W M, Cremers Cor W R J, Devilee Peter, Dinjens Winand N M, de Krijger Ronald R, Robledo Merced
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes.
Clinical endocrinology 2013 Dec 79 (6): 817-23.
P?czkowska Mariola, Kowalska Aldona, Sygut Jacek, Waligórski Dariusz, Malinoc Angelica, Janaszek-Sitkowska Hanna, Prejbisz Aleksander, Januszewicz Andrzej, Neumann Hartmut P
Profiling of somatic mutations in phaeochromocytoma and paraganglioma by targeted next generation sequencing analysis.
International journal of endocrinology 2015 2015 138573.
Luchetti Andrea, Walsh Diana, Rodger Fay, Clark Graeme, Martin Tom, Irving Richard, Sanna Mario, Yao Masahiro, Robledo Mercedes, Neumann Hartmut P H, Woodward Emma R, Latif Farida, Abbs Stephen, Martin Howard, Maher Eamonn
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