A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes

Genomics

Volumn 13, Issue 4, 1992, Pages 917-924

  Driscoll, Daniel J ^a   Waters, Michael F ^a   Williams, Charles A ^a   Zori, Roberto T ^a   Glenn, Christopher C ^a   Avidano, Karen M ^a   Nicholls, Robert D ^a  

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

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 15Q; CHROMOSOME DELETION; CONTROLLED STUDY; DNA DETERMINATION; DNA METHYLATION; FEMALE; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; HUMAN CELL; LEUKOCYTE; MAJOR CLINICAL STUDY; MALE; PARENT; PRADER WILLI SYNDROME; SEX;

BLOTTING, SOUTHERN; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA; DNA PROBES; FEMALE; HUMAN; MALE; MENTAL RETARDATION; METHYLATION; MOVEMENT DISORDERS; PARENTS; PRADER-WILLI SYNDROME; SEX FACTORS; SUPPORT, NON-U.S. GOV'T; SYNDROME;

MAMMALIA;

EID: 0026700732     PISSN: 08887543     EISSN: 10898646     Source Type: Journal    
DOI: 10.1016/0888-7543(92)90001-9     Document Type: Article

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