Hypomethylation of the H19 gene causes not only silver-russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

American Journal of Human Genetics

Volumn 78, Issue 4, 2006, Pages 604-614

  Bliek, Jet ^a   Terhal, Paulien ^b   Van Den Bogaard, Marie José ^b   Maas, Saskia ^a   Hamel, Ben ^c   Salieb Beugelaar, Georgette ^a   Simon, Marleen ^d   Letteboer, Tom ^b   Van Der Smagt, Jasper ^b   Kroes, Hester ^b   Mannens, Marcel ^a  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^d ERASMUS MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHILD; CHROMOSOME 11P; CHROMOSOME MARKER; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DNA METHYLATION; FEMALE; GENE MUTATION; GIGANTISM; GROWTH RETARDATION; H19 GENE; HEMIHYPERTROPHY; HUMAN; INFANT; INTRAUTERINE GROWTH RETARDATION; MALE; MULTIPLE MALFORMATION SYNDROME; NEWBORN; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; PREGNANCY; PRIORITY JOURNAL; SILVER RUSSELL SYNDROME; SOUTHERN BLOTTING; TUMOR SUPPRESSOR GENE;

EID: 33645463808     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/502981     Document Type: Article

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