Frequency of WT1 and 11p15 constitutional aberrations and phenotypic correlation in childhood Wilms tumour patients

European Journal of Cancer

Volumn 48, Issue 17, 2012, Pages 3249-3256

  Segers, H ^a   Kersseboom, R ^b   Alders, M ^c   Pieters, R ^a   Wagner, A ^b   Van Den Heuvel Eibrink, M M ^a  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c ACADEMIC MEDICAL CENTER   (Netherlands)

Author keywords

11p15; Genotype; Phenotype; Wilms tumour; WT1

Indexed keywords

WT1 PROTEIN;

ARTICLE; BECKWITH WIEDEMANN SYNDROME; CANCER PATIENT; CHILD; CHILDHOOD CANCER; CHROMOSOME 11P; CHROMOSOME ABERRATION; CLINICAL ASSESSMENT; COHORT ANALYSIS; DENYS DRASH SYNDROME; FEMALE; GENE LOCUS; GENETIC COUNSELING; GENOTYPE PHENOTYPE CORRELATION; HEMIHYPERTROPHY; HIGH RESOLUTION MELTING ANALYSIS; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; NEPHROBLASTOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SOUTHERN BLOTTING; WAGR SYNDROME;

CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 11; FEMALE; GENES, WILMS TUMOR; GENOTYPE; HUMANS; INFANT; KIDNEY NEOPLASMS; MALE; PHENOTYPE; WILMS TUMOR;

EID: 84868211253     PISSN: 09598049     EISSN: 18790852     Source Type: Journal    
DOI: 10.1016/j.ejca.2012.06.008     Document Type: Article

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