Expression and imprinting of MAGEL2 suggest a role in Prader-Willi syndrome and the homologous murine imprinting phenotype

Human Molecular Genetics

Volumn 9, Issue 12, 2000, Pages 1813-1819

  Lee, Syann ^a   Kozlov, Serguei ^b   Hernandez, Lidia ^b   Chamberlain, Stormy J ^c   Brannan, Camilynn I ^c   Stewart, Colin L ^b   Wevrick, Rachel ^a  

^a UNIVERSITY OF ALBERTA   (Canada)

^b NATIONAL CANCER INSTITUTE   (United States)

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

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN; BRAIN DEVELOPMENT; CELL DIFFERENTIATION; CELL VIABILITY; CHROMOSOME 15Q; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; EMBRYO; FEMALE; FETUS (ANATOMY); GENE EXPRESSION; GENE LOCATION; GENOME IMPRINTING; IN SITU HYBRIDIZATION; MOUSE; MUSCLE HYPOTONIA; NONHUMAN; NORTHERN BLOTTING; OBESITY; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALIA; MURINAE; RODENTIA;

EID: 0033852735     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/9.12.1813     Document Type: Article

References (21)

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