Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

Epigenetics

Volumn 8, Issue 10, 2013, Pages 1053-1060

  Calvello, Mariarosaria ^a   Tabano, Silvia ^a,b   Colapietro, Patrizia ^b   Maitz, Silvia ^c   Pansa, Alessandra ^b   Augello, Claudia ^b   Lalatta, Faustina ^a   Gentilin, Barbara ^a   Spreafico, Filippo ^d   Calzari, Luciano ^e   Perotti, Daniela ^d   Larizza, Lidia ^b,e   Russo, Silvia ^e   Selicorni, Angelo ^c   Sirchia, Silvia M ^a,b   Miozzo, Monica ^a,b  

^a FONDAZIONE IRCCS CA GRANDA OSPEDALE MAGGIORE POLICLINICO   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c SAN GERARDO HOSPITAL   (Italy)

^d NATIONAL CANCER INSTITUTE   (Italy)

^e ISTITUTO AUXOLOGICO ITALIANO   (Italy)

Author keywords

BWS; DNA methylation; Genomic imprinting; Pyrosequencing; UPD

Indexed keywords

ABDOMINAL WALL DEFECT; ADOLESCENT; AMNION FLUID ANALYSIS; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CANCER SUSCEPTIBILITY; CHILD; CHROMOSOME 11P; CLINICAL ARTICLE; CONTROLLED STUDY; DNA METHYLATION; FEMALE; GENE; GENE EXPRESSION; GENETIC DISORDER; GENOME IMPRINTING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; ICR1 GENE; ICR2 GENE; INFANT; MALE; OMPHALOCELE; PERIPHERAL LYMPHOCYTE; PRENATAL DIAGNOSIS; PYROSEQUENCING; UNIPARENTAL DISOMY;

BWS; DNA METHYLATION; GENOMIC IMPRINTING; PYROSEQUENCING; UPD;

BECKWITH-WIEDEMANN SYNDROME; CHILD; CHILD, PRESCHOOL; DNA METHYLATION; EPIGENESIS, GENETIC; FEMALE; FETAL DISEASES; GENOMIC IMPRINTING; HERNIA, UMBILICAL; HUMANS; INFANT; MALE; PHENOTYPE;

EID: 84884967377     PISSN: 15592294     EISSN: 15592308     Source Type: Journal    
DOI: 10.4161/epi.25812     Document Type: Article

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