Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesis
- 1 July 1995
- journal article
- research article
- Published by Springer Nature in Human Genetics
- Vol. 96 (1) , 102-104
- https://doi.org/10.1007/bf00214195
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.Journal of Medical Genetics, 1993
- A familial mutation in the testis-determining gene SRY shared by both sexesHuman Genetics, 1992
- Constitutional mutations in the WT1 gene in patients with Denys-Drash syndromeHuman Molecular Genetics, 1992
- WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumourNature, 1991
- A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motifNature, 1990
- The candidate Wilms' tumour gene is involved in genitourinary developmentNature, 1990
- An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumorCell, 1990
- Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locusCell, 1990
- [31] Detection and localization of single base changes by denaturing gradient gel electrophoresisPublished by Elsevier ,1987
- A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal diseaseThe Journal of Pediatrics, 1970