Corrections to Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes [J Med Genet, 51, (2014) 229-38] DOI:10.1136/jmedgenet-2013-102116;Genome-wide DNA methylation analysis of patients with imprinting disorders identifies differentially methylated regions associated with novel candidate imprinted genes

Journal of Medical Genetics

Volumn 51, Issue 4, 2014, Pages 229-238

  Docherty, Louise E ^a,b   Rezwan, Faisal I ^a   Poole, Rebecca L ^a,b   Jagoe, Hannah ^a   Lake, Hannah ^a   Lockett, Gabrielle A ^a   Arshad, Hasan ^a,c   Wilson, David I ^a   Holloway, John W ^a   Temple, I Karen ^a,d   Mackay, Deborah J G ^a,b  

^a UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^b SALISBURY NHS FOUNDATION TRUST   (United Kingdom)

^c David Hyde allergy centre Isle of Wight   (United Kingdom)

^d PRINCESS ANNE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; BECKWITH WIEDEMANN SYNDROME; BIPOLAR DISORDER; CLINICAL FEATURE; CONTROLLED STUDY; DNA METHYLATION; DOWN SYNDROME; EPIGENETICS; EXTRACHROMOSOMAL INHERITANCE; FEMALE; FOLLOW UP; GENE EXPRESSION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC DISORDER; GENOME IMPRINTING; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; PSEUDOHYPOPARATHYROIDISM; PSEUDOHYPOPARATHYROIDISM 1B; QUALITY CONTROL; SILVER RUSSELL SYNDROME; YOUNG ADULT;

EPIGENETICS; GENOME-WIDE; IMPRINTING;

ALLELES; BECKWITH-WIEDEMANN SYNDROME; CPG ISLANDS; DIABETES MELLITUS; DNA METHYLATION; GENE EXPRESSION REGULATION; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENOME, HUMAN; GENOMIC IMPRINTING; HUMANS; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; REPRODUCIBILITY OF RESULTS; RIBONUCLEOPROTEINS, SMALL NUCLEAR;

EID: 84896327297     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2012-101203corr1     Document Type: Erratum

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