Non-recurrent 17p11.2 deletions are generated by homologous and non-homologous mechanisms

Human Genetics

Volumn 116, Issue 1-2, 2005, Pages 1-7

  Shaw, Christine J ^a   Lupski, James R ^a,b  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b TEXAS CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; CELL LINE; CHROMOSOME 17P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DNA SEQUENCE; GENE DELETION; GENE LOCATION; GENE STRUCTURE; HOMOLOGOUS RECOMBINATION; HUMAN; HUMAN CELL; HYBRID CELL; LYMPHOBLAST; MOLECULAR MECHANICS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 17; HUMANS; MOLECULAR SEQUENCE DATA; RECOMBINATION, GENETIC; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION;

EID: 11244287233     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-004-1204-9     Document Type: Article

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