Identification of the human/mouse syntenic common fragile site FRA7K/Fra12C1 - Relation of FRA7K and other human common fragile sites on chromosome 7 to evolutionary breakpoints

International Journal of Cancer

Volumn 120, Issue 1, 2007, Pages 48-54

  Helmrich, Anne ^a,b,d   Stout Weider, Karen ^b   Matthaei, Anja ^a   Hermann, Klaus ^c   Heiden, Thomas ^b   Schrock, Evelin ^a  

^a DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^b HUMBOLDT UNIVERSITY   (Germany)

^c Signature Diagnostics AG   (Germany)

^d INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

Chromosome rearrangements; Common fragile site; Fra12C1; FRA7K; IMMP2l immp21

Indexed keywords

ANIMAL CELL; ARTICLE; CANCER CELL CULTURE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 7; CHROMOSOME FRAGILE SITE; CHROMOSOME MAP; CHROMOSOME REARRANGEMENT; CONTROLLED CLINICAL TRIAL; DNA HELIX; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENE AMPLIFICATION; GENE DUPLICATION; HUMAN; HUMAN CELL; LMMP21 GENE; MOLECULAR EVOLUTION; MOUSE; NONHUMAN; PRIORITY JOURNAL; SYNTENY;

ANIMALS; BREAST NEOPLASMS; CHROMOSOME BREAKAGE; CHROMOSOME FRAGILE SITES; CHROMOSOME FRAGILITY; CHROMOSOME MAPPING; CHROMOSOMES, ARTIFICIAL, YEAST; CHROMOSOMES, HUMAN, PAIR 7; DATABASES, GENETIC; EVOLUTION, MOLECULAR; GENE AMPLIFICATION; GENOME; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; MICE; MICE, INBRED BALB C; MICE, INBRED C57BL; SPLEEN; SYNTENY;

EID: 33845424480     PISSN: 00207136     EISSN: 10970215     Source Type: Journal    
DOI: 10.1002/ijc.22049     Document Type: Article

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