Prader-Willi and Angelman syndromes: Sister imprinted disorders

American Journal of Medical Genetics - Seminars in Medical Genetics

Volumn 97, Issue 2, 2000, Pages 136-146

  Cassidy, Suzanne B ^a   Dykens, Elisabeth ^b   Williams, Charles A ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NONE

Author keywords

Angelman syndrome; Behavioral phenotype; Chromosome disorder; Genetic imprinting; Mental retardation; Microdeletion; Prader Willi syndrome; Uniparental disomy

Indexed keywords

RIBONUCLEOPROTEIN; UBIQUITIN;

ARTICLE; BEHAVIOR; CHROMOSOME 15Q; CHROMOSOME DISORDER; CHROMOSOME MAP; CLINICAL FEATURE; COGNITIVE DEFECT; ENDOCRINE DISEASE; GENE CONTROL; GENE EXPRESSION; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; HYPOTHALAMUS DISEASE; MENTAL DEFICIENCY; OBSESSION; PATHOGENESIS; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; PROTEIN DEGRADATION; RNA SPLICING; TARGET CELL; UNIPARENTAL DISOMY;

ANGELMAN SYNDROME; ANIMALS; DISEASE MODELS, ANIMAL; FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; PRADER-WILLI SYNDROME;

ANIMALIA; ATAXIA;

EID: 0033651946     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(200022)97:2<136::AID-AJMG5>3.0.CO;2-V     Document Type: Article

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