WT1 mutation as a cause of 46 XY DSD and Wilm's tumour: A case report and literature review

Acta Paediatrica, International Journal of Paediatrics

Volumn 100, Issue 7, 2011, Pages

  Dai, Yang Li ^a   Fu, Jun Fen ^a   Hong, Fang ^a   Xu, Shan ^a   Shen, Zheng ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

Disorder of sexual development; Wilms' tumour

Indexed keywords

CHORIONIC GONADOTROPIN; ESTRADIOL; FOLLITROPIN; GENOMIC DNA; LUTEINIZING HORMONE; PROLACTIN; TESTOSTERONE; WT1 PROTEIN;

ADOLESCENT; CASE REPORT; CODON; CONTROLLED STUDY; DNA SEQUENCE; ESTRADIOL BLOOD LEVEL; ESTROGEN THERAPY; EXON; FEMALE; FOLLITROPIN BLOOD LEVEL; GENE INSERTION; GONADAL DYSGENESIS; HUMAN; HUMAN TISSUE; LUTEINIZING HORMONE BLOOD LEVEL; MUTATIONAL ANALYSIS; NEPHRECTOMY; NEPHROBLASTOMA; PRIORITY JOURNAL; PROLACTIN BLOOD LEVEL; REVIEW; STOP CODON; TESTOSTERONE BLOOD LEVEL; THROMBOCYTOPENIA;

46, XY DISORDERS OF SEX DEVELOPMENT; ADOLESCENT; EXONS; FEMALE; GENES, WILMS TUMOR; HUMANS; KIDNEY NEOPLASMS; MUTAGENESIS, INSERTIONAL; WILMS TUMOR;

EID: 79958023683     PISSN: 08035253     EISSN: 16512227     Source Type: Journal    
DOI: 10.1111/j.1651-2227.2011.02167.x     Document Type: Review

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