Assignment of human putative tumor suppressor genes ST13 (alias SNC6) and ST14 (alias SNC19)to human chromosome bands 22q13 and 11q24→q25 by in situ hybridization

Cytogenetics and Cell Genetics

Volumn 83, Issue 1-2, 1998, Pages 56-57

  Zhang, Y ^a,b   Cai, X ^a   Schlegelberger, B ^b   Zheng, S ^a  

^a ZHEJIANG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b UNIVERSITY OF KIEL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; DNA;

ARTICLE; CHROMOSOME 11Q; CHROMOSOME 22Q; DNA LIBRARY; GENE MAPPING; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE HOMOLOGY; TUMOR SUPPRESSOR GENE; CHROMOSOME 11; CHROMOSOME 22; CHROMOSOME MAP; COLON TUMOR; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; MOLECULAR CLONING;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 22; CLONING, MOLECULAR; COLONIC NEOPLASMS; DNA, NEOPLASM; GENES, TUMOR SUPPRESSOR; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE;

EID: 0032217136     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

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