Fine mapping genetic determinants of the highly variably expressed MHC gene ZFP57

European Journal of Human Genetics

Volumn 22, Issue 4, 2014, Pages 568-571

  Plant, Katharine ^a   Fairfax, Benjamin P ^a   Makino, Seiko ^a   Vandiedonck, Claire ^a,b,c   Radhakrishnan, Jayachandran ^a   Knight, Julian C ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b INSERM   (France)

^c UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Disease susceptibility; Expression quantitative trait; Genetic variation; MHC; ZFP57

Indexed keywords

ACP1 GENE; ARTICLE; BEHAVIOR DISORDER; CHILD; CHROMOSOME 2P; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 2P25; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE; GENOTYPE; HUMAN; HYPERPHAGIA; INTELLECTUAL IMPAIRMENT; MICROSATELLITE MARKER; MYT1L GENE; OBESITY; PRESCHOOL CHILD; PRIORITY JOURNAL; PXDN GENE; SCHOOL CHILD; SH3HYL1 GENE; SINGLE NUCLEOTIDE POLYMORPHISM; SNTG2 GENE; TMEM18 GENE; TPO GENE;

ACQUIRED IMMUNODEFICIENCY SYNDROME; AUTOIMMUNE DISEASES; CHROMOSOME MAPPING; DEOXYRIBONUCLEASE I; DNA METHYLATION; EPIGENESIS, GENETIC; GENE EXPRESSION REGULATION; GENES, MHC CLASS I; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOMIC IMPRINTING; HUMANS; KRUPPEL-LIKE TRANSCRIPTION FACTORS; LINKAGE DISEQUILIBRIUM; NEOPLASMS; POLYMORPHISM, SINGLE NUCLEOTIDE; QUANTITATIVE TRAIT LOCI; REPRESSOR PROTEINS; ZINC FINGERS;

EID: 84896543537     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2013.244     Document Type: Article

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