A necropsy case of Denys-Drash syndrome with a WT1 mutation in exon 7.

Journal of medical genetics

Volumn 39, Issue 8, 2002, Pages

  Fukuzawa, R ^a   Sakamoto, J ^a   Heathcott, R W ^a   Hata, J I ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

WT1 PROTEIN;

ARTICLE; CASE REPORT; CHILD; DENYS DRASH SYNDROME; ECHOGRAPHY; EXON; FATALITY; FEMALE; GENETICS; HUMAN; INFANT; MUTATION; PATHOLOGY; TUMOR SUPPRESSOR GENE;

CHILD; DENYS-DRASH SYNDROME; EXONS; FATAL OUTCOME; FEMALE; GENES, WILMS TUMOR; HUMANS; INFANT; MUTATION; WT1 PROTEINS;

MLCS; MLOWN;

EID: 0036676135     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.39.8.e48     Document Type: Article

References (0)