(Q28209893)

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Testicular position in the androgen insensitivity syndrome: implications for the role of androgens in testicular descent

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A stochastic model of temporally regulated generation of oligodendrocytes in cell culture.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Functional characterization of naturally occurring mutant androgen receptors from subjects with complete androgen insensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Studies of the androgen receptor in dispersed fibroblasts: investigation of patients with androgen insensitivity.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Testicular feminization: a model for testicular descent in mice and men

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Single amino acid substitution (840Arg-->His) in the hormone-binding domain of the androgen receptor leads to incomplete androgen insensitivity syndrome associated with a thermolabile androgen receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

The diagnosis of 5 alpha-reductase deficiency in infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A clinical overview of WT1 gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion: indication of gene localization

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Wilms' tumor 1 and Dax-1 modulate the orphan nuclear receptor SF-1 in sex-specific gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Cryptorchidism in mice mutant for Insl3

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Constitutional and somatic mutations in theWTI gene in wilms' tumor patients

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Dihydrotestosterone and Its Relationship to Testosterone in Infancy and Childhood*

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Stochastic mechanism of cellular aging--abrupt telomere shortening as a model for stochastic nature of cellular aging

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

1 reference

7 January 2021

Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Pituitary-Gonadal Relations in Infancy: 2. Patterns of Serum Gonadal Steroid Concentrations in Man from Birth to Two Years of Age

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021

Targeted disruption of the Insl3 gene causes bilateral cryptorchidism

1 reference

https://api.crossref.org/works/10.1016%2FS0303-7207%2801%2900631-1

7 January 2021