Genetic proof of unequal meiotic crossovers in reciprocal deletion and duplication of 17p11.2

American Journal of Human Genetics

Volumn 71, Issue 5, 2002, Pages 1072-1081

  Shaw, Christine J ^a   Bi, Weimin ^a   Lupski, James R ^a,b,c  

^a Departments of Molecular and Human Genetics   (United States)

^b BAYLOR COLLEGE OF MEDICINE   (United States)

^c Texas Children's Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 17P; CHROMOSOME MAP; CROSSING OVER; DNA FLANKING REGION; DNA STRAND BREAKAGE; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENETIC RECOMBINATION; HAPLOTYPE; HUMAN; HUMAN TISSUE; MEIOSIS; PHENOTYPE; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

EID: 0036842833     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/344346     Document Type: Article

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