The mechanisms involved in formation of deletions and duplications of 15qll-ql3

Journal of Medical Genetics

Volumn 35, Issue 2, 1998, Pages 130-136

  Robinson, V P ^a   Dutly, F ^a   Nicholls, R D ^b   Bernasconi, F ^c   Penaherrera, M ^c   Michaelis, R C ^d   Abeliovich, D ^e   Schinzel, A A ^f  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF ZURICH   (Switzerland)

^c UNIVERSITY HOSPITALS OF CLEVELAND   (United States)

^d Greenwood Genetic Center   (United States)

^e HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^f UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

Angelman syndrome; Deletion; Duplication 15qll ql3; Prader willi s>tidrome

Indexed keywords

DNA MARKER;

ARTICLE; CHROMOSOME 15Q; CROSSING OVER; GENE DELETION; GENE DUPLICATION; GENE REARRANGEMENT; GENETIC RECOMBINATION; HAPLOTYPE; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ANGELMAN SYNDROME; CHROMOSOME BREAKAGE; CHROMOSOMES, HUMAN, PAIR 15; DNA PROBES; ELECTROPHORESIS, POLYACRYLAMIDE GEL; FEMALE; GENE DELETION; GENETIC MARKERS; GENOMIC IMPRINTING; HAPLOTYPES; HUMANS; MALE; MEIOSIS; MICROSATELLITE REPEATS; MULTIGENE FAMILY; PRADER-WILLI SYNDROME; RECOMBINATION, GENETIC; SISTER CHROMATID EXCHANGE;

EID: 0031981973     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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