Epigenetic deregulation of imprinting in congenital diseases of aberrant growth

BioEssays

Volumn 28, Issue 5, 2006, Pages 453-459

  Delaval, Katia ^a   Wagschal, Alexandre ^a   Feil, Robert ^a  

^a CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; CONGENITAL DISORDER; DIABETES MELLITUS; DNA METHYLATION; EPIGENETICS; GENE CONTROL; REVIEW; SILVER RUSSELL SYNDROME;

BECKWITH-WIEDEMANN SYNDROME; CHROMOSOMES, HUMAN, PAIR 11; DIABETES MELLITUS; DNA METHYLATION; EPIGENESIS, GENETIC; FEMALE; GENOMIC IMPRINTING; GROWTH DISORDERS; HUMANS; INFANT, NEWBORN; MALE; MODELS, GENETIC; PREGNANCY; SYNDROME;

EID: 33646346610     PISSN: 02659247     EISSN: None     Source Type: Journal    
DOI: 10.1002/bies.20407     Document Type: Review

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