LOH on chromosome 11q, but not SDHD and Men1 mutations was frequently detectable in chinese patients with pheochromocytoma and paraganglioma

Endocrine

Volumn 30, Issue 3, 2006, Pages 307-312

  Sun, Hai Yan ^a,b   Cui, Bin ^a,b   Su, Din Wei ^a   Jin, Xiao Long ^a   Sun, Fu Kang ^a   Zu, Yu ^a   Jiang, Lei ^a   Wang, Wei Qing ^a,b   Ning, Guang ^a,b  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

^b SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

Loss of heterozygosity; Mutation; Pheochromocytoma; Tumor suppressor gene

Indexed keywords

SUCCINATE DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 11Q; CHROMOSOME LOSS; CLINICAL ARTICLE; FEMALE; GENE FREQUENCY; GENE FUNCTION; GENE LOCUS; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PARAGANGLIOMA; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 34347358627     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-006-0009-0     Document Type: Article

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