MBD3 mutations are not responsible for ICR1 hypomethylation in Silver-Russell syndrome

European Journal of Medical Genetics

Volumn 53, Issue 1, 2010, Pages 23-24

  Bachmann, Nadine ^a   Spengler, Sabrina ^a   Binder, Gerhard ^b   Eggermann, Thomas ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

METHYL CPG BINDING PROTEIN; METHYL CPG BINDING PROTEIN 3; UNCLASSIFIED DRUG;

ARTICLE; CLINICAL ARTICLE; DNA DETERMINATION; GENE MUTATION; GENE SEQUENCE; GENOME IMPRINTING; HUMAN; IMPRINTED CONTROL REGION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; POSTNATAL GROWTH; PROTEIN METHYLATION; SILVER RUSSELL SYNDROME;

ABNORMALITIES, MULTIPLE; CHROMOSOMES, HUMAN, PAIR 11; DNA METHYLATION; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; GENOMIC IMPRINTING; HUMANS; MUTATION; SILVER-RUSSELL SYNDROME;

MUS;

EID: 74149084808     PISSN: 17697212     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejmg.2009.12.002     Document Type: Article

References (7)

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6. Reese K.J., Lin S., Verona R.I., Schultz R.M., and Bartolomei M. Maintenance of paternal methylation and repression of the imprinted H19 gene requires Mbd3. Plos Genet. 3 (2007) e137
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