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Volumn 30, Issue 1, 1996, Pages 269-286
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Atypical presentation of Denys-Drash syndrome in a female with a novel Wt1 gene mutation.
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
DNA BINDING PROTEIN;
TRANSCRIPTION FACTOR;
WT1 PROTEIN;
ZINC FINGER PROTEIN;
AMINO ACID SEQUENCE;
BINDING SITE;
CASE REPORT;
CHILD;
CHRONIC KIDNEY FAILURE;
CONGENITAL MALFORMATION;
EXON;
FEMALE;
FEMALE GENITAL SYSTEM;
GENETICS;
HUMAN;
KIDNEY;
KIDNEY TUMOR;
MOLECULAR GENETICS;
MUTATION;
NEPHROBLASTOMA;
NUCLEOTIDE SEQUENCE;
PATHOLOGY;
PHENOTYPE;
PRENATAL DEVELOPMENT;
REVIEW;
SYNDROME;
TUMOR SUPPRESSOR GENE;
AMINO ACID SEQUENCE;
BASE SEQUENCE;
BINDING SITES;
CHILD;
DNA;
DNA-BINDING PROTEINS;
EXONS;
FEMALE;
GENES, WILMS TUMOR;
GENITALIA, FEMALE;
HUMANS;
KIDNEY;
KIDNEY FAILURE, CHRONIC;
KIDNEY NEOPLASMS;
MOLECULAR SEQUENCE DATA;
MUTATION;
PHENOTYPE;
SYNDROME;
TRANSCRIPTION FACTORS;
WILMS TUMOR;
WT1 PROTEINS;
ZINC FINGERS;
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EID: 0030339762
PISSN: 05476844
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
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Times cited : (6)
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References (29)
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