The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders

Clinical Genetics

Volumn 79, Issue 2, 2011, Pages 169-175

  Bourque, D K ^a,b   Penaherrera M S ^a,b   Yuen, R K C ^a,b   Van Allen, M I ^a   Mcfadden, D E ^a,b   Robinson, W P ^a,b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b UNIVERSITY OF BRITISH COLUMBIA   (Canada)

Author keywords

11p15.5; DNA methylation; Imprinting; KvDMR1; Triploidy

Indexed keywords

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CHROMOSOME 11P; CHROMOSOME ABERRATION; COMPLETE HYDATIDIFORM MOLE; CONTROLLED STUDY; DNA METHYLATION; GENE; GENE SEQUENCE; HUMAN; MAJOR CLINICAL STUDY; MEST GENE; PLACENTA DISORDER; PLACENTAL MESENCHYMAL DYSPLASIA; PRIORITY JOURNAL; SGCE GENE; SNRPN GENE; TRIPLOIDY;

CHROMOSOMES, HUMAN, PAIR 11; DNA METHYLATION; FEMALE; FETAL DISEASES; GENOMIC IMPRINTING; HUMANS; MOLECULAR DIAGNOSTIC TECHNIQUES; PLACENTA DISEASES; POTASSIUM CHANNELS, VOLTAGE-GATED; PREGNANCY; SEQUENCE ANALYSIS, DNA;

EID: 78650867109     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2010.01443.x     Document Type: Article

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