Non-random asynchronous replication at 22q11.2 favours unequal meiotic crossovers leading to the human 22q11.2 deletion

Journal of Medical Genetics

Volumn 41, Issue 6, 2004, Pages 413-420

  Baumer, A ^a   Riegel, M ^a   Schinzel, A ^a  

^a UNIVERSITY OF ZURICH   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CELL CYCLE S PHASE; CELL NUCLEUS; CHROMOSOME 22Q; CHROMOSOME NOR; CLINICAL ARTICLE; CROSSING OVER; DNA FLANKING REGION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE LOCUS; GENE REPLICATION; GENE TRANSLOCATION; GENOME IMPRINTING; HUMAN; INTERPHASE; MALE; MEIOSIS; NUCLEOTIDE REPEAT; PRIORITY JOURNAL; STATISTICAL SIGNIFICANCE;

EID: 2942709617     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.2003.016352     Document Type: Article

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