Russell-Silver syndrome due to paternal H19/IGF2 hypomethylation in a patient conceived using intracytoplasmic sperm injection

Reproductive BioMedicine Online

Volumn 20, Issue 6, 2010, Pages 843-847

  Chopra, M ^a,b   Amor, D J ^c,d   Sutton, L ^e   Algar, E ^c,d   Mowat, D ^a,b  

^a SYDNEY CHILDREN'S HOSPITAL   (Australia)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

^c MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^d UNIVERSITY OF MELBOURNE   (Australia)

^e ROYAL HOSPITAL FOR WOMEN   (Australia)

Author keywords

Assisted reproductive technology; Imprinting disorders; Russell Silver syndrome

Indexed keywords

RNA H19; SOMATOMEDIN B;

ALLELE; ARTICLE; CASE REPORT; DNA METHYLATION; EPIGENETICS; FEEDING DISORDER; FEMALE; GENE LOCUS; GENE MUTATION; GENOTYPE; HUMAN; INFANT; INTRACYTOPLASMIC SPERM INJECTION; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PATENT DUCTUS ARTERIOSUS; SEMEN ANALYSIS; SILVER RUSSELL SYNDROME;

EID: 77957790511     PISSN: 14726483     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.rbmo.2010.02.025     Document Type: Article

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