Epigenetic detection of human chromosome 14 uniparental disomy

Human Mutation

Volumn 22, Issue 1, 2003, Pages 92-97

  Murphy, S K ^a   Wylie, A A ^a,b   Coveler, K J ^c   Cotter, P D ^d   Papenhausen, P R ^e   Sutton, V R ^c   Shaffer, L G ^c   Jirtle, R L ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b ASTRAZENECA   (United Kingdom)

^c BAYLOR COLLEGE OF MEDICINE   (United States)

^d CHILDREN S HOSPITAL OAKLAND   (United States)

^e LABORATORY CORPORATION OF AMERICA   (United States)

Author keywords

Bisulfite sequencing; DLK1; GTL2; Imprinted gene; MEG3; Methylation; Methylation specific PCR; Monochromosomal hybrid; Uniparental disomy

Indexed keywords

DNA;

ARTICLE; CHROMOSOME 14; DLK1 GENE; GENE; GENE EXPRESSION REGULATION; GENOME IMPRINTING; MEG3 GENE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE; UNIPARENTAL DISOMY;

CHROMOSOMES, HUMAN, PAIR 14; DNA; FETUS; GENETIC MARKERS; GENOMIC IMPRINTING; GLYCOPROTEINS; HUMANS; LIVER; NONDISJUNCTION, GENETIC; NUCLEIC ACID AMPLIFICATION TECHNIQUES; POLYMERASE CHAIN REACTION; PROTEINS; RETROSPECTIVE STUDIES; SEQUENCE ANALYSIS, DNA; SULFITES; UNIPARENTAL DISOMY;

EID: 0038384954     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.10237     Document Type: Article

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