Genomic imbalances in pediatric patients with chronic kidney disease

Journal of Clinical Investigation

Volumn 125, Issue 5, 2015, Pages 2171-2178

  Verbitsky, Miguel ^a   Sanna Cherchi, Simone ^a   Fasel, David A ^a   Levy, Brynn ^a   Kiryluk, Krzysztof ^a   Wuttke, Matthias ^b   Abraham, Alison G ^c   Kaskel, Frederick ^d   Köttgen, Anna ^b,c   Warady, Bradley A ^e   Furth, Susan L ^f   Wong, Craig S ^g   Gharavi, Ali G ^a  

^a Department of Neurology and the Taub Institute for Research on Alzheimer's Disease and the Aging Brain   (United States)

^b UNIVERSITY OF FREIBURG   (Germany)

^c JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^d ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

^e CHILDREN S MERCY HOSPITAL   (United States)

^f UNIVERSITY OF PENNSYLVANIA   (United States)

^g UNIVERSITY OF NEW MEXICO SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEPATOCYTE NUCLEAR FACTOR 1; HEPATOCYTE NUCLEAR FACTOR 1 HOMEOBOX B; UNCLASSIFIED DRUG;

47,XXX SYNDROME; ADULT; ARTICLE; CHILD; CHILDHOOD DISEASE; CHROMOSOMAL MICROARRAY; CHROMOSOME 17P; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHRONIC KIDNEY DISEASE; CLINICAL ASSESSMENT; CLINICAL EVALUATION; COHORT ANALYSIS; CONTROLLED STUDY; COPY NUMBER VARIATION; ETHNIC DIFFERENCE; GENE DISRUPTION; GENETIC COUNSELING; GENOMIC IMBALANCE; GENOMICS; GENOTYPE; GLOMERULUS FILTRATION RATE; HUMAN; KIDNEY DEVELOPMENT; KIDNEY FUNCTION; LONGITUDINAL STUDY; MAJOR CLINICAL STUDY; MICROARRAY ANALYSIS; OBSERVATIONAL STUDY; PENETRANCE; PLEIOTROPY; POINT MUTATION; PREVALENCE; PRIORITY JOURNAL; PROSPECTIVE STUDY; RISK FACTOR; SEX DIFFERENCE; ADOLESCENT; CHROMOSOME DISORDERS; CHRONIC KIDNEY FAILURE; CLINICAL TRIAL; EPIDEMIOLOGY; FEMALE; GENE DELETION; GENE DOSAGE; GENETICS; HUMAN CHROMOSOME; INFANT; MALE; MULTICENTER STUDY; NEWBORN; PRESCHOOL CHILD; UNITED STATES;

ADOLESCENT; CAUSALITY; CHILD; CHILD, PRESCHOOL; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN; FEMALE; GENE DOSAGE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MICROARRAY ANALYSIS; PREVALENCE; PROSPECTIVE STUDIES; RENAL INSUFFICIENCY, CHRONIC; SEQUENCE DELETION; UNITED STATES;

EID: 84929000152     PISSN: 00219738     EISSN: 15588238     Source Type: Journal    
DOI: 10.1172/JCI80877     Document Type: Article

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