DNA hypomethylation, transient neonatal diabetes, and prune belly sequence in one of two identical twins

European Journal of Pediatrics

Volumn 169, Issue 2, 2010, Pages 207-213

  Laborie, Lene Bjerke ^a,b   Mackay, Deborah J G ^c,d   Temple, I Karen ^c,e   Molven, Anders ^a,b   Søvik, Oddmund ^b   Njølstad, Pal Rasmus ^a,b  

^a HAUKELAND UNIVERSITY HOSPITAL   (Norway)

^b UNIVERSITY OF BERGEN   (Norway)

^c UNIVERSITY OF SOUTHAMPTON   (United Kingdom)

^d SALISBURY DISTRICT HOSPITAL   (United Kingdom)

^e UNIVERSITY HOSPITAL SOUTHAMPTON NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

Chromosome 6; DNA methylation; Imprinting anomaly; Neonatal diabetes; Prune belly syndrome

Indexed keywords

AUTOANTIBODY; HEPATOCYTE NUCLEAR FACTOR 1ALPHA; HEPATOCYTE NUCLEAR FACTOR 1BETA; HEPATOCYTE NUCLEAR FACTOR 3BETA; INWARDLY RECTIFYING POTASSIUM CHANNEL SUBUNIT KIR6.2; PROTEIN ABCC8; PROTEIN GCK; PROTEIN IPF1; PROTEIN ZFP57; PROTEIN ZIC3; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR PAX4; UNCLASSIFIED DRUG;

ABDOMINAL WALL MUSCULATURE; ARTICLE; CASE REPORT; CHEMICAL ANALYSIS; CHILD; CHROMOSOME 6Q; CLINICAL FEATURE; CRYPTORCHISM; DIABETES MELLITUS; DNA METHYLATION; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; MALE; MESODERM; MICROSATELLITE MARKER; MOLECULAR GENETICS; MONOZYGOTIC TWINS; NEWBORN; NEWBORN DISEASE; PRIORITY JOURNAL; PRUNE BELLY SYNDROME; URINARY TRACT MALFORMATION;

CHROMOSOMES, HUMAN, PAIR 6; DIABETES MELLITUS; DISEASES IN TWINS; DNA; DNA METHYLATION; DNA MUTATIONAL ANALYSIS; GENETIC MARKERS; HUMANS; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MALE; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; TWINS, MONOZYGOTIC;

EID: 77949423607     PISSN: 03406199     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00431-009-1008-y     Document Type: Article

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