Chromosome 11 monosomy in conjunction with a mutated SDHD initiation codon in nonfamilial paraganglioma cases

Cancer Genetics and Cytogenetics

Volumn 150, Issue 2, 2004, Pages 128-135

  Riemann, Kathrin ^a   Sotlar, Karl ^b   Kupka, Susan ^a   Braun, Simone ^a   Zenner, Hans Peter ^a   Preyer, Serena ^a   Pfister, Markus ^a,c   Pusch, Carsten M ^a   Blin, Nikolaus ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^c STANFORD UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA; PARAFFIN; SATELLITE DNA;

ADULT; AGED; ARTICLE; CASE REPORT; CENTROMERE; CHROMOSOME 11; CODON; CONTROLLED STUDY; DNA DETERMINATION; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE MUTATION; GENE SEQUENCE; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MALE; MONOSOMY; PARAGANGLIOMA; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; AGED; AGED, 80 AND OVER; BASE SEQUENCE; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CODON, INITIATOR; ELECTRON TRANSPORT COMPLEX II; EXONS; FEMALE; GENETIC MARKERS; HUMANS; MALE; PARAGANGLIOMA; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 1842454038     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2003.10.013     Document Type: Article

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