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A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8128316

A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

About this item

Full title

A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

Publisher

United States: John Wiley & Sons, Inc

Journal title

Journal of clinical laboratory analysis, 2021-05, Vol.35 (5), p.e23769-n/a

Language

English

Formats

Publication information

Publisher

United States: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Objective
Denys‐Drash syndrome (DDS) is defined by the triad of Wilms tumor, nephrotic syndrome, and/or ambiguous genitalia. Genetic testing may help identify new gene mutation sites and play an important role in clinical decision‐making.
Methods
We present a patient with an XY karyotype and female appearance, nephropathy, and Wilms tumor...

Alternative Titles

Full title

A novel WT1 gene mutation in a chinese girl with denys‐drash syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8128316

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8128316

Other Identifiers

ISSN

0887-8013

E-ISSN

1098-2825

DOI

10.1002/jcla.23769

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