Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)

Human Molecular Genetics

Volumn 8, Issue 6, 1999, Pages 1025-1037

  Christian, Susan L ^a   Fantes, Judy A ^a   Mewborn, Stephanie K ^a   Huang, Bing ^b   Ledbetter, David H ^a  

^a UNIVERSITY OF CHICAGO   (United States)

^b GENZYME GENETICS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 15Q; CHROMOSOME 16P; CONTROLLED STUDY; EXPRESSED SEQUENCE TAG; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DUPLICATION; GENE MAPPING; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; MONKEY; NUCLEOTIDE SEQUENCE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PSEUDOGENE; SEQUENCE HOMOLOGY; SEQUENCE TAGGED SITE; YEAST ARTIFICIAL CHROMOSOME;

ANGELMAN SYNDROME; ANIMALS; BACTERIA; BACTERIOPHAGES; CERCOPITHECIDAE; CHROMOSOME FRAGILITY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; CLONING, MOLECULAR; CONTIG MAPPING; DNA; DNA, COMPLEMENTARY; GENE DOSAGE; GENE DUPLICATION; GENE LIBRARY; HOMINIDAE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MOLECULAR SEQUENCE DATA; PRADER-WILLI SYNDROME; SEQUENCE ANALYSIS, DNA; SEQUENCE DELETION; SEQUENCE TAGGED SITES;

CERCOPITHECIDAE; PRIMATES;

EID: 0032971379     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.6.1025     Document Type: Article

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