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Volumn 30, Issue 13, 2012, Pages
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Von hippel-lindau disease and erythrocytosis
a a a a a a a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ALLELE;
ARTICLE;
CASE REPORT;
CHROMOSOME 10;
CHROMOSOME 3;
DNA DETERMINATION;
ERYTHROCYTOSIS;
EXON;
FLUORESCENCE IN SITU HYBRIDIZATION;
GENE;
GENE MUTATION;
HETEROZYGOSITY;
HUMAN;
HUMAN CELL;
MALE;
NUCLEOTIDE SEQUENCE;
PHEOCHROMOCYTOMA;
PRIORITY JOURNAL;
SYMPTOM;
VHL GENE;
VON HIPPEL LINDAU DISEASE;
ADRENAL TUMOR;
BIOPSY;
BLOOD;
GENETIC PREDISPOSITION;
GENETICS;
MUTATION;
PEDIGREE;
PHENOTYPE;
PHLEBOTOMY;
POLYCYTHEMIA;
TREATMENT OUTCOME;
ACETYLSALICYLIC ACID;
ANTICOAGULANT AGENT;
BIOLOGICAL MARKER;
ERYTHROPOIETIN;
VHL PROTEIN, HUMAN;
VON HIPPEL LINDAU PROTEIN;
ADRENAL GLAND NEOPLASMS;
ADULT;
ANTICOAGULANTS;
ASPIRIN;
BIOLOGICAL MARKERS;
BIOPSY;
DNA MUTATIONAL ANALYSIS;
ERYTHROPOIETIN;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
IN SITU HYBRIDIZATION, FLUORESCENCE;
MALE;
MUTATION;
PEDIGREE;
PHENOTYPE;
PHEOCHROMOCYTOMA;
PHLEBOTOMY;
POLYCYTHEMIA;
TREATMENT OUTCOME;
VON HIPPEL-LINDAU DISEASE;
VON HIPPEL-LINDAU TUMOR SUPPRESSOR PROTEIN;
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EID: 84862984243
PISSN: 0732183X
EISSN: 15277755
Source Type: Journal
DOI: 10.1200/JCO.2011.38.6797 Document Type: Article |
Times cited : (17)
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References (10)
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