Minimal definition of the imprinting center and fixation of a chromosome 15q11-q13 epigenotype by imprinting mutations

Proceedings of the National Academy of Sciences of the United States of America

Volumn 93, Issue 15, 1996, Pages 7811-7815

  Saitoh, Shinji ^a,g   Buiting, Karin ^b   Rogan, Peter K ^c,h   Buxton, Jessica L ^d   Driscoll, Daniel J ^e   Arnemann, Joachim ^f   König, Rainer ^f   Malcolm, Sue ^d   Horsthemke, Bernhard ^b   Nicholls, Robert D ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY HOSPITAL ESSEN   (Germany)

^c PENN STATE COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY COLLEGE LONDON   (United Kingdom)

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

^f GOETHE UNIVERSITY   (Germany)

^g HOKKAIDO UNIVERSITY   (Japan)

^h ALLEGHENY SINGER RESEARCH INSTITUTE   (United States)

Author keywords

Angelman syndrome; DNA methylation; gametogenesis; monoallelic expression; Prader Willi syndrome

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 15Q; CLINICAL ARTICLE; DNA METHYLATION; FAMILY; FEMALE; GAMETOGENESIS; GENE DELETION; GENE MUTATION; GENOME IMPRINTING; GENOTYPE; HAPPY PUPPET SYNDROME; HUMAN; MALE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; SIBLING;

ANGELMAN SYNDROME; BASE SEQUENCE; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA PRIMERS; FAMILY; FEMALE; GENETIC MARKERS; GENOMIC IMPRINTING; HOMOZYGOTE; HUMANS; MALE; METHYLATION; MOLECULAR SEQUENCE DATA; MOTHERS; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PRADER-WILLI SYNDROME; SEQUENCE DELETION; TRANSCRIPTION, GENETIC;

RICKETTSIA SP. PAR;

EID: 16044365355     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.15.7811     Document Type: Article

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