Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome

American Journal of Medical Genetics, Part A

Volumn 152 A, Issue 10, 2010, Pages 2521-2528

  Lin, Shin Yu ^a,b   Lee, Chien Nan ^b   Hung, Chia Cheng ^c   Tsai, Wen Yu ^b   Lin, Shuan Pei ^d   Li, Ni Chung ^b   Hsieh, Wu Shiun ^b   Tung, Yi Ching ^b   Niu, Dau Ming ^e   Hsu, Wen Ming ^b   Chen, Lang Yao ^b   Fang, Mei Ya ^a,b   Tu, Mei Pin ^b   Kuo, Pei Wen ^a,b   Lin, Chiou Ya ^b   Su, Yi Ning ^b,c   Ho, Hong Nerng ^b,c  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^d MACKAY MEMORIAL HOSPITAL   (Taiwan)

^e TAIPEI VETERANS GENERAL HOSPITAL   (Taiwan)

Author keywords

Array CGH; H19 gene; Microdeletion; Silver Russell syndrome; UPD(7)mat

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 13Q; CHROMOSOME 14Q; CHROMOSOME 15Q; CHROMOSOME 1Q; CHROMOSOME 7; CHROMOSOME 7P; CLINICAL ARTICLE; CONTROLLED STUDY; DIFFERENTIALLY METHYLATED REGION; DNA METHYLATION; DNA STRUCTURE; EPIGENETICS; GENE; GENE DELETION; GENE DOSAGE; GENE MUTATION; GENOME ANALYSIS; H19 GENE; HETEROZYGOSITY LOSS; HUMAN; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; MULTIPLEX POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SILVER RUSSELL SYNDROME; UNIPARENTAL DISOMY; BLOOD; CHROMOSOME 12; DNA MICROARRAY; GENE AMPLIFICATION; GENE EXPRESSION PROFILING; GENETIC VARIABILITY; GENETICS; GENOME IMPRINTING; ISOLATION AND PURIFICATION; METHODOLOGY; POLYMERASE CHAIN REACTION; SINGLE NUCLEOTIDE POLYMORPHISM;

DNA; MESODERM SPECIFIC TRANSCRIPT PROTEIN; PROTEIN; RNA H19; UNTRANSLATED RNA;

CHROMOSOMES, HUMAN, PAIR 12; DNA; DNA METHYLATION; GENE AMPLIFICATION; GENE EXPRESSION PROFILING; GENETIC VARIATION; GENOMIC IMPRINTING; HUMANS; LOSS OF HETEROZYGOSITY; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RNA, UNTRANSLATED; SEQUENCE DELETION; SILVER-RUSSELL SYNDROME;

EID: 78349261200     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.33629     Document Type: Article

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