Modification of 15q11 - q13 DNA methylation imprints in unique angelman and prader - willi patients

Human Molecular Genetics

Volumn 2, Issue 9, 1993, Pages 1377-1382

  Glenn, Christopher C ^a   Nicholls, Robert D ^a   Robinson, Wendy P ^b   Saitoh, Shinjl ^a,c   Nllkawa, Norlo ^c   Schlnzel, Albert ^b   Horsthemke, Bernhard ^d   Driscoll, Daniel J ^a  

^a UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^b UNIVERSITY OF ZURICH   (Switzerland)

^c NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d UNIVERSITY HOSPITAL ESSEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 15Q; CHROMOSOME REARRANGEMENT; CONTROLLED STUDY; DNA METHYLATION; FEMALE; GENE; GENE LOCUS; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; INTERSTITIAL CHROMOSOME DELETION; MALE; PRADER WILLI SYNDROME;

ANGELMAN SYNDROME; CHROMOSOMES, HUMAN, PAIR 15; DNA; FEMALE; GENE DELETION; GENE REARRANGEMENT; GENETIC MARKERS; HUMAN; MALE; METHYLATION; PEDIGREE; PHENOTYPE; PRADER-WILLI SYNDROME; SUPPORT, NON-U.S. GOV'T;

EID: 0027169927     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/2.9.1377     Document Type: Article

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