Implications of COMT long-range interactions on the phenotypic variability of 22q11.2 deletion syndrome.

Nucleus (Austin, Tex.)

Volumn 4, Issue 6, 2013, Pages 487-493

  Zeitz, Michael J ^a   Lerner, Paula P ^a   Ay, Ferhat ^a   Van Nostrand, Eric ^a   Heidmann, Julia D ^a   Noble, William S ^a   Hoffman, Andrew R ^a  

^a UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CATECHOL METHYLTRANSFERASE; COMT PROTEIN, HUMAN; TRANSCRIPTOME;

ARTICLE; B LYMPHOCYTE; CELL LINE; CHROMOSOME CONFORMATION CAPTURE; CHROMOSOME DELETION; CHROMOSOME MAP; CLUSTER ANALYSIS; CYTOLOGY; DIGEORGE SYNDROME; FIBROBLAST; GENE EXPRESSION; GENETIC VARIABILITY; GENETICS; GENOME ANALYSIS; HUMAN; LONG-RANGE INTERACTIONS; METABOLISM; PHENOTYPE; SCHIZOPHRENIA;

CHROMOSOME CONFORMATION CAPTURE; DIGEORGE SYNDROME; GENOME ORGANIZATION; LONG-RANGE INTERACTIONS; SCHIZOPHRENIA;

B-LYMPHOCYTES; CATECHOL O-METHYLTRANSFERASE; CELL LINE; CHROMOSOME DELETION; CHROMOSOME MAPPING; CLUSTER ANALYSIS; DIGEORGE SYNDROME; FIBROBLASTS; GENE EXPRESSION; GENETIC VARIATION; HUMANS; PHENOTYPE; TRANSCRIPTOME;

EID: 84902130550     PISSN: None     EISSN: 19491042     Source Type: Journal    
DOI: 10.4161/nucl.27364     Document Type: Article

References (0)