WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin

Human Genetics

Volumn 93, Issue 2, 1994, Pages 115-120

  Nordenskjöld, Agneta ^a,b   Friedman, Eitan ^a   Anvret, Maria ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b ST GÖRAN S HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ASPARTIC ACID; HISTIDINE;

ALLELE; ARTICLE; CANCER RISK; CHROMOSOME 11P; CLINICAL ARTICLE; DENYS DRASH SYNDROME; EXON; FEMALE; GENE LOSS; GENE MUTATION; GENETIC MARKER; GENETIC POLYMORPHISM; HUMAN; HUMAN CELL; KIDNEY DISEASE; MALE; NEPHROBLASTOMA; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PSEUDOHERMAPHRODITISM; TUMOR SUPPRESSOR GENE;

ALLELES; BASE SEQUENCE; CHROMOSOMES, HUMAN, PAIR 11; DNA; DNA PRIMERS; EXONS; FEMALE; GENES, WILMS TUMOR; HUMAN; KIDNEY NEOPLASMS; MALE; MOLECULAR SEQUENCE DATA; NEPHROBLASTOMA; PARENTS; POINT MUTATION; PSEUDOHERMAPHRODITISM; SUPPORT, NON-U.S. GOV'T; SYNDROME; ZINC FINGERS;

EID: 0028091340     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/BF00210593     Document Type: Article

References (25)

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