A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneity

Pediatric Nephrology

Volumn 23, Issue 4, 2008, Pages 587-595

  Conte, Maria Luisa ^a,b   Bertoli Avella, Aida M ^a   de Graaf, Bianca M ^a   Punzo, Francesca ^b   Lama, Giuliana ^b   La Manna, Angela ^b   Grassia, Carolina ^b   Rambaldi, Pier Francesco ^b   Oostra, Ben A ^a   Perrotta, Silverio ^b  

^a ERASMUS MEDICAL CENTER   (Netherlands)

^b SECOND UNIVERSITY OF NAPLES   (Italy)

Author keywords

Complex disorder; Genetic linkage; Primary familial vesicoureteral reflux; VUR

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 1; CHROMOSOME 1P; CHROMOSOME 22Q; CHROMOSOME 3; CHROMOSOME 3Q; CHROMOSOME 4; CONTROLLED STUDY; FAMILIAL DISEASE; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC IDENTIFICATION; GENETIC MARKER; GENETIC SCREENING; GENOME ANALYSIS; HAPLOTYPE; HUMAN; ITALY; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROMOTER REGION; VESICOURETERAL REFLUX;

ADOLESCENT; ADULT; AGED; CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 3; DNA MUTATIONAL ANALYSIS; FAMILY; FAMILY HEALTH; FEMALE; GENETIC HETEROGENEITY; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; HUMANS; INFANT; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; PEDIGREE; VESICO-URETERAL REFLUX;

EID: 40549090957     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-007-0675-z     Document Type: Article

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