Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation.

scientific article published on 24 July 2009

Clinical and molecular overview of inherited disorders resulting from epigenomic dysregulation. is …
instance of (P31):
review articleQ7318358
scholarly articleQ13442814

External links are
P356DOI10.1016/J.EJMG.2009.07.004
P698PubMed publication ID19632366

P50authorAlbertina De SarioQ73074684
P2093author name stringAlbertina De Sario
P2860cites workDNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian developmentQ22010765
P433issue6
P304page(s)363-372
P577publication date2009-07-24
P1433published inEuropean Journal of Medical GeneticsQ15817083
P1476titleClinical and molecular overview of inherited disorders resulting from epigenomic dysregulation
P478volume52

Reverse relations

cites work (P2860)
Q33640084Chromatin remodeling in development and disease: focus on CHD7.
Q36253442DNA replication is altered in Immunodeficiency Centromeric instability Facial anomalies (ICF) cells carrying DNMT3B mutations
Q29619753Epigenetic modifications and human disease
Q37997085Histone-modifying enzymes: regulators of developmental decisions and drivers of human disease.
Q35940736Severity of eating disorder symptoms related to oxytocin receptor polymorphisms in anorexia nervosa.
Q24607321Spectrum of MLL2 (ALR) mutations in 110 cases of Kabuki syndrome
Q39232068The Social Security Administration's Compassionate Allowances Initiative: Condition Spotlight on Rubinstein-Taybi Syndrome
Q37225239The clinical utilization of circulating cell free DNA (CCFDNA) in blood of cancer patients

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