A set of duplicons on human chromosome 9 is involved in the origin of a supernumerary marker chromosome

Genomics

Volumn 87, Issue 6, 2006, Pages 747-757

  Paulis, Marianna ^a   Bensi, Mirella ^a   Moralli, Daniela ^a   De Carli, Luigi ^a   Raimondi, Elena ^a  

^a UNIVERSITY OF PAVIA   (Italy)

Author keywords

Chromosome evolution; Chromosome instability; Chromosome rearrangements; Duplicons; Genome plasticity; Human chromosome 9; Meiotic exchanges; Somatic exchanges

Indexed keywords

ARTICLE; CHROMOSOME 9; CHROMOSOME 9P; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DATA BASE; FLUORESCENCE IN SITU HYBRIDIZATION; GENOME; GERM CELL; HUMAN; HUMAN CELL; MARKER CHROMOSOME; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PARALOGY; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SOMATIC CELL; SUPERNUMERARY CHROMOSOME; CHROMOSOMAL INSTABILITY; DUPLICATE GENE; GENE REARRANGEMENT; GENETIC MARKER; GENETICS; MOLECULAR EVOLUTION; NUCLEOTIDE REPEAT;

DNA;

BASE SEQUENCE; CHROMOSOMAL INSTABILITY; CHROMOSOMES, HUMAN, PAIR 9; DNA; EVOLUTION, MOLECULAR; GENE REARRANGEMENT; GENES, DUPLICATE; GENETIC MARKERS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; REPETITIVE SEQUENCES, NUCLEIC ACID;

EID: 33746505978     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/j.ygeno.2006.02.014     Document Type: Article

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