Exploratory investigation on functional significance of ETS2 and SIM2 genes in Down syndrome

Disease Markers

Volumn 31, Issue 5, 2011, Pages 247-257

  Chatterjee, Arpita ^a   Dutta, Samikshan ^a,b   Sinha, Swagata ^a   Mukhopadhyay, Kanchan ^a  

^a Manovikas Biomedical Research and Diagnostic Centre   (India)

^b Dongguk University College of Medicine   (South Korea)

Author keywords

Down syndrome; ETS2; SIM2; transcriptional regulation

Indexed keywords

E26 ONCOGENE HOMOLOG 2 PROTEIN; GENOMIC DNA; LEUCINE; METHIONINE; SINGLE MINDED 2 PROTEIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CHROMOSOME 21; CONTROLLED STUDY; DOWN SYNDROME; FEMALE; GENE FREQUENCY; GENE INTERACTION; GENE LINKAGE DISEQUILIBRIUM; GENETIC RISK; GENOTYPE; HAPLOTYPE; HETEROZYGOSITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MEIOSIS; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 80955139749     PISSN: 02780240     EISSN: 18758630     Source Type: Journal    
DOI: 10.3233/DMA-2011-0825     Document Type: Article

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